ライフサイエンスコーパス: intergenic

1 of all transcription (genic, intragenic, and intergenic).

2 tein-coding genes, and the rest appear to be intergenic.

3 Ss) were annotated as noncoding, with 24% in intergenic, 12% in promoters, and 28% in introns, with s

4 protein-coding hosts or neighbours, some are intergenic and independent.

5 ncing data from 268 patients to catalog gene-intergenic and intergenic-intergenic fusions and charact

6 Intergenic and intragenic enhancers found inside topolog

7 e to WGS data because of the large number of intergenic and intron regions that consist of a massive

8 ctly binds LSD1 and recruits it primarily to intergenic and intronic enhancers.

9 al variants (SVs), including those targeting intergenic and intronic non-coding regions that eluded p

10 BMI1 was highly enriched at intergenic and pericentric heterochromatin, co-immunopre

11 he complete mitochondrial genome and nuclear intergenic and protein-coding sequences were obtained by

12 We noted that the intergenic and upstream sites are located in the distal

13 to identify 4 riboswitches, 13 trans-acting (intergenic), and 22 cis-acting (antisense) small RNAs (t

14 s in different regions of the genome (genic, intergenic, and heterochromatic) and at different distan

15 DNA is preferentially hypomethylated within intergenic areas and LINE1 promoter areas of the genome.

16 aralleled coverage of coding, non-coding and intergenic areas of both nuclear and mitochondrial genom

17 II are detected at gene-coding as well as at intergenic areas when double-strand breaks (DSBs) are in

18 However, fusions often occur with intergenic breakpoints, and the role of such fusions has

19 We report a novel intergenic breast cancer risk locus containing an enhanc

20 further characterize the genomic features of intergenic cheRNA (icheRNA) and their similarity to enha

21 uterus PGR showed far more tendency to bind intergenic chromatin regions and low evidence of interac

22 dentify a novel long noncoding RNA Noncoding Intergenic Co-Induced transcript (NICI) on chromosome 12

23 n (PCR) analyses: Enterobacterial Repetitive Intergenic Consensus (ERIC) and Random Amplified Polymor

24 n HSPCs from EGF-treated mice, but increased intergenic copy number variant mutations were detected.

25 in regulatory pathway that connects aberrant intergenic CpG methylation to human neoplastic and devel

26 f methylation in the heart, enriched in lone intergenic CpGs and depleted from CpG islands around gen

27 ory linkage appears to have resulted from an intergenic deletion in eutherians that significantly alt

28 control the establishment and maintenance of intergenic DNA methylation remain poorly understood.

29 schemes to obtain the best performance over intergenic DNA sequence data.

30 tant tumours also exhibit hypomethylation of intergenic DNA.

31 bodies and a reduction in the methylation of intergenic DNA.

32 iated H3K27me3 accumulate initially at large intergenic domains that can then spread into genes only

33 as those predicted from base-pair changes in intergenic enhancer sites, coding-region variants, and S

34 dent on high STAT5 levels as a result of the intergenic enhancer.

35 400Kb upstream to IGFBP5, which overlaps an intergenic ERalpha-bound enhancer that loops to the IGFB

36 kpoints were partitioned into intragenic and intergenic events.

37 spatially and categorically; (ii) coding and intergenic features are recapitulated at high resolution

38 lucidate the potential oncogenic function of intergenic fusions and highlight the wide-ranging conseq

39 , RSPO3, and PIK3CA-can be generated by gene-intergenic fusions through splicing of the intervening r

40 ers lack H3K27me3, and it is unknown whether intergenic H3K27me3 deposits affect nearby genes.

41 Excess intergenic H3K27me3 in both TF-deficient tissues is asso

42 lti-exonic transcripts from 561 intronic and intergenic haploblocks associated with 392 traits and di

43 ognized the iamR promoter (P(iamR) ) and the intergenic iamP-iamA region (P(iamP-A) ).

44 unique sequence derived from the prrF1-prrF2 intergenic (IG) sequence (the PrrHIG sequence).

45 negatively impacted or increased by the HN-L intergenic insertion.

46 268 patients to catalog gene-intergenic and intergenic-intergenic fusions and characterize their imp

47 We focused on the long intergenic/intervening ncRNAs (lincRNAs), hidden within

48 of 54,875 bacterial genomes identified 4686 intergenic invertible DNA regions (invertons), revealing

49 The intergenic IRES of Cricket Paralysis Virus (CrPV-IRES) f

50 nal significance of this region, which being intergenic is probably regulatory.

51 ECONEXIN was the most highly conserved intergenic lncRNA containing 83.0% homology with the mou

52 Given that intergenic lncRNA have substantially less sequence conse

53 an experimental reannotation of the GENCODE intergenic lncRNA populations in matched human and mouse

54 The current study identified a novel intergenic lncRNA, LINC00461 (ECONEXIN) using a combined

55 Conversely, intergenic lncRNAs (lincRNAs) and eRNAs have lower capac

56 Genome-wide analyses of intergenic lncRNAs (lincRNAs) revealed that lincRNA spli

57 genes across species, evolutionary conserved intergenic lncRNAs are likely to be functional.

58 ification of these lncRNAs reveals that most intergenic lncRNAs originate from enhancers rather than

59 ic class of RNAs that includes, for example, intergenic lncRNAs, antisense transcripts, and enhancer

60 atterns, and uncovers two notable classes of intergenic lncRNAs: one showing strong purifying selecti

61 in the genome, predominantly expressed from intergenic loci, and associated with antiviral or DNA da

62 and CD, IL12RB2, IRF1/SLC22A5, STAT3 and an intergenic locus at 6p21.31.

63 rmed on human left/right pairs identified an intergenic long noncoding RNA adjacent to the PITX2 gene

64 d provides accurate TSS prediction for human intergenic miRNAs at a high resolution.

65 PRO-seq experiments identified TSSs for 480 intergenic miRNAs, indicating a wide usage of alternativ

66 A screen to identify intergenic mutations that allow for sss1(ts) cells to gr

67 The challenge of linking intergenic mutations to target genes has limited molecul

68 ings identify Neat1 as a p53-regulated large intergenic ncRNA (lincRNA) with a key role in suppressin

69 f a newly identified vast class of very long intergenic non-coding (vlinc) RNAs.

70 LincRNA-p21 is a long intergenic non-coding RNA (lincRNA) involved in the p53-

71 hibit distinct messenger RNA (mRNA) and long intergenic non-coding RNA (lincRNA) profiles compared to

72 In this study, we present data that long intergenic non-coding RNA 346 (LINC00346) functions as a

73 In patients with type 2 diabetes, long intergenic non-coding RNA predicting cardiac remodeling

74 ication and characterization of a novel long intergenic non-coding RNA with MyoD-regulated and skelet

75 Long intergenic non-coding RNA-Nucleotide Metabolism Regulato

76 Long intergenic non-coding RNAs (lincRNAs) are emerging as in

77 Long intergenic non-coding RNAs (lincRNAs) are transcribed fr

78 ematic investigation of the capacity of long intergenic non-coding RNAs (lincRNAs) as biomarkers asso

79 Long intergenic non-coding RNAs (lincRNAs) have been identifi

80 Long intergenic non-coding RNAs (lincRNAs) have been implicat

81 atment of cancer, the interplay between long intergenic non-coding RNAs (lncRNAs) and chromatin remod

82 h increased expression of LRRK2 and two long intergenic non-coding RNAs (lncRNAs), LINC02555 and AC07

83 transcriptome to detect 6,701 putative long intergenic non-coding transcripts (lincRNAs) expressed i

84 deletion-based approach identified two long intergenic non-coding(linc)RNAs, lincRNA-Cox2 and lincRN

85 Expression of long intergenic non-protein coding RNA 518 (LINC00518) and pr

86 d carcinoma-associated STAT3-activating long intergenic non-protein coding transcript (PRECSIT).

87 in brain expression of a human-specific long intergenic noncoding RNA (LINC01268; GRCh37/hg19: LOC285

88 o the A-bodies by interacting with ribosomal intergenic noncoding RNA (rIGSRNA).

89 tive cardiac lncRNAs, including LIPCAR (long intergenic noncoding RNA predicting cardiac remodeling a

90 the prior postmortem association of the long intergenic noncoding RNA specifically with suicide by vi

91 ong noncoding RNA (lncRNA) Flicr (Foxp3 long intergenic noncoding RNA) is a negative regulator that t

92 While long intergenic noncoding RNAs (lincRNAs) and mRNAs share sim

93 Long intergenic noncoding RNAs (lincRNAs) are derived from th

94 Long intergenic noncoding RNAs (lincRNAs) are emerging as imp

95 Long intergenic noncoding RNAs (lincRNAs) are important regul

96 Long intergenic noncoding RNAs (lincRNAs) are increasingly re

97 Long intergenic noncoding RNAs (lincRNAs) are increasingly re

98 Long intergenic noncoding RNAs (lincRNAs) are long noncoding

99 Long intergenic noncoding RNAs (lincRNAs) can regulate the tr

100 xtent to which alternative splicing and long intergenic noncoding RNAs (lincRNAs) contribute to the s

101 Prioritising long intergenic noncoding RNAs (lincRNAs) for functional char

102 ese noncoding RNAs, a growing number of long intergenic noncoding RNAs (lincRNAs) have been described

103 Long intergenic noncoding RNAs (lincRNAs) play important role

104 e shield prevents Pol I from producing sense intergenic noncoding RNAs (sincRNAs) that can disrupt nu

105 fic regulation of protein-coding genes, long intergenic noncoding RNAs and microRNAs.

106 previously unreported fusions involving long intergenic noncoding RNAs, demonstrating a previously un

107 protein-coding genes, and 567 putative long intergenic noncoding RNAs.

108 Among intergenic nucleosomes, repair activity is elevated on t

109 These contacts are orchestrated by intergenic olfactory receptor enhancers, the 'Greek isla

110 HPRT1 function was robust to deletion of any intergenic or deeply intronic non-coding region, indicat

111 Genic and intergenic parallel evolution occur particularly in anti

112 exit the nucleus with diverse intragenic and intergenic poly(A)-tail lengths.

113 erein as non-3UTR), as well as antisense and intergenic polyadenlation.

114 ealed that changes in gene expression due to intergenic polymorphisms are associated with longevity a

115 among populations was largely attributed to intergenic recombination.

116 was recruited by the cricket paralysis virus intergenic region (CrPV IGR) IRES to form a stable 40S-I

117 The intergenic region (IGR) IRES adopts an unusual structure

118 some, we took advantage of the IRES from the intergenic region (IGR) of the Cricket Paralysis Virus.

119 ide (nt) deletion (Delta39) in the noncoding intergenic region (IGR) of the viral large (L) segment t

120 We have recently shown that the noncoding intergenic region (IGR) present in each arenavirus genom

121 It contains trpR, an intergenic region (IGR), and the biosynthetic trpB and t

122 on and a point mutation within the L-segment intergenic region (IGR), and three silent changes in the

123 located in 5 untranslated region (uPSS) and intergenic region (iPSS), respectively.

124 regions located in the C1 ORF and around the intergenic region (IR).

125 RH50 binds to transcripts of the 23S-4.5S intergenic region and, in its absence, levels of the cor

126 A genes, 22 transfer RNA genes and an 834 bp intergenic region assumed to be the D-loop.

127 between coronary artery disease (CAD) and an intergenic region at locus 9p21.3.

128 One of these, at chromosome 11p13, is an intergenic region between Ets homologous factor (EHF) an

129 A unique target is found in the intergenic region between genes encoding the nitric oxid

130 Further characterization of the intergenic region between genomic regions of GATA6-AS1 a

131 ated within a predicted super-enhancer in an intergenic region between HLA-DRB1 and HLA-DQA1, localiz

132 regions go through substantial changes: the intergenic region between NP and VP35, as well as the fi

133 pts involving parts of PPP3R1, CNRIP1 and an intergenic region between PLEK and CNRIP1, in the blood

134 Tandem repeats were frequently found in the intergenic region between the prophage at the 3' end and

135 IRES of Israeli acute paralysis virus (IAPV) intergenic region captures and redirects translating rib

136 G, NID1, DHRS12, ITPK1, ACSF3, TNFRSF13C and intergenic region chr10p12.31 was replicated in a cohort

137 sion from a novel promoter element within an intergenic region flanked by trpR and trpB.

138 The most significant locus was in an intergenic region in chromosome 17, rs12453010, having P

139 ), HDL-cholesterol (PHOSPHO1, SYNGAP1 and an intergenic region in chromosome 2) and triglycerides (MY

140 single-nucleotide polymorphisms (SNPs) in an intergenic region located between the oncogenes MYC and

141 ing disruptive missense RVs of NPC1L1 and an intergenic region near APOC1P1 associated with low-densi

142 One of them, located in the intergenic region of APOBEC3B and APOBEC3C, showed evide

143 .71 x 10(-10), rs16891982), and revealed the intergenic region of BEND7 and PRPF18 as a novel locus a

144 The SNP rs17645023 located in the intergenic region of CACNG4 and CACNG5 was identified to

145 An intergenic region of human chromosome 2 (2p25.3) harbors

146 Linc-RAM is transcribed from an intergenic region of myogenic cells and its expression i

147 ription start site was identified within the intergenic region of the miR-183 cluster, which may regu

148 t cancer risk is strongly associated with an intergenic region on 11q13.

149 gnificant associations at two novel loci: an intergenic region on 9p21.3 (rs12553324, P = 5.87 x 10 (

150 nflammatory states, maps to the 5' end of an intergenic region on Chr11p13 that is implicated as a mo

151 ree loci located in GABBR2, RUFY3, and in an intergenic region on chromosome 2 replicated with the sa

152 olymorphisms (SNPs) (r(2)>0.9) located in an intergenic region on chromosome 3q26 were associated wit

153 ignificant loci were identified including an intergenic region on chromosome 9 that has previously be

154 pendent reporter gene cassette located in an intergenic region remained silent, indicating that the t

155 S_NmUC isolates was an IS1301 element in the intergenic region separating the capsule ctr-css operons

156 NA genome, with an 827 nt-long 5' UTR and an intergenic region separating two open reading frames.

157 d and confirmed a one-nucleotide indel in an intergenic region that significantly alters global trans

158 ind Cbf1p in vivo targets and a Tye7p target intergenic region to be bound by Cbf1p.

159 gulator in Chlamydia, can bind to the trpRBA intergenic region upstream of the alternative trpBA prom

160 ontrol is mediated by binding of MarA to the intergenic region upstream of the ycgZ-ymgABC operon.

161 Six of these genes and 1 intergenic region were new discoveries showing different

162 4.8 kb miR-183 family cluster, including the intergenic region which contains highly conserved genomi

163 We show that XdhR binds the xdhABC-xdhR intergenic region with high affinity (Kd approximately 0

164 us PecS binds two sites within the pecS-pecM intergenic region with K(d) = 0.3 +/- 0.1 nM, a binding

165 omosome reporters, we discovered that the 5' intergenic region, introns 2 and 6 of human telomerase g

166 n of a 198-nucleotide sequence into the HN-L intergenic region, resulting in reduced viral gene expre

167 We applied this methodology to the HBS1L-MYB intergenic region, which is associated with red-blood-ce

168 with a transposon insertion in the upstream intergenic region, while FT2c and FT2d obtained a transp

169 ressive histone mark H3K9me3 in the Il2-Il21 intergenic region.

170 s), and 68 meningococci had the capsule-null intergenic region.

171 lated by a bidirectional promoter within the intergenic region.

172 en inserted into each isolate at a conserved intergenic region.

173 Nontranslated intergenic regions (IGRs) compose 10-15% of bacterial ge

174 the most abundant sRNAs transcribed from the intergenic regions (IGRs) of the bacterial genome.

175 elated X chromosome variants were located in intergenic regions (n = 397).

176 CFAP45, AFF3, TP73, UBCLP1, RPL13P, and two intergenic regions (p values < 0.0001 were confirmed usi

177 tioned rice genome showed that regulatory or intergenic regions account for the most trait heritabili

178 border regions between domains contain large intergenic regions and a high density of transcription f

179 ct to motifs, targeting to promoter/intronic intergenic regions and chromatin folding.

180 on and 23 mutations, most of which locate to intergenic regions and insertion sequences.

181 we show that BORDER proteins are enriched in intergenic regions and prevent interference between clos

182 so reveal putative novel initiation sites in intergenic regions and within genes.

183 (rRNA) processing, many coding sequences and intergenic regions appeared to be direct targets of RNas

184 ty of identified pA sites were mapped to the intergenic regions downstream of previously annotated EB

185 The majority of risk loci are in intergenic regions for which functional mechanism(s) rem

186 DNAm sites located in intergenic regions had a higher mean DNAm level and were

187 transmembrane domains, and that thymine-rich intergenic regions harbor a widespread potential to prod

188 that control pervasive transcription within intergenic regions have not been well established.

189 f somatic mutation across exons, introns and intergenic regions highlights the repertoire of cancer g

190 These SNPs were distributed in genic and intergenic regions in the eight pseudomolecules of the p

191 ong noncoding transcripts (>200 nt) from the intergenic regions of annotated protein-coding genes.

192 ensive transcriptional activity occurring in intergenic regions of genomes has raised the question wh

193 heory based sigma70 model indicates that the intergenic regions of salt-responsive genes are enriched

194 ensity of sigma70 promoter-like sites in the intergenic regions of salt-responsive genes drives the R

195 several CpG sites primarily localized in the intergenic regions of the genome.

196 ferentially distributed over gene bodies and intergenic regions of the genome.

197 we developed a custom script that can detect intergenic regions of the S. pyogenes genome.

198 r 44 traits studied are novel and located in intergenic regions or introns of genes.

199 regulated loci correspond to transposons and intergenic regions producing 24-nucleotide siRNAs that g

200 BCG1, CPT1A, MYLIP, TXNIP and SLC7A11) and 2 intergenic regions showed differential methylation in as

201 ase on the X-chromosome, and an elevation in intergenic regions suggesting that chromatin structure m

202 cted, nucleotide diversity is much higher in intergenic regions than within gene bodies (regions span

203 ng use of an alternative genetic code, large intergenic regions that are highly expressed and up to 3

204 evising several methods to select subsets of intergenic regions that can concentrate these rare RNA c

205 Our signatures driven by CpGs in intergenic regions that showed substantial overlap with

206 icient resolution in the larger intronic and intergenic regions to identify copy number changes.

207 DMRs located within intergenic regions were heavily enriched for AP-1 transc

208 We also identified intergenic regions where methylation is associated with

209 Stringtie was then performed to identify the intergenic regions whose expression was influenced by th

210 Intergenic regions within the unique long 52 gene (UL52;

211 It has few transposable elements, tiny intergenic regions, and is remarkably intron-poor, as mo

212 l coding sequences, complex genomic regions, intergenic regions, and methylation motifs revealed smal

213 bserve that the genome is more accessible in intergenic regions, and that increased accessibility is

214 introns), while being depleted in coding and intergenic regions, and these findings may have biologic

215 ber of genes, together with transcripts from intergenic regions, are up-regulated.

216 t may be transcribed: coding, noncoding, and intergenic regions, as well as repetitive elements, telo

217 ion in CpG island (CGI) and demethylation in intergenic regions, defined as 'backbone', largely vary

218 Approximately 1500 intergenic regions, displaying low DNA methylation, high

219 ften, 24-nt-dominated siRNA loci occurred in intergenic regions, especially at the 5'-flanking region

220 ociated haplotype blocks are in intronic and intergenic regions, hindering their functional evaluatio

221 While most termini were found in intergenic regions, numerous abundant termini were also

222 nt along the telomere-centromere axis in the intergenic regions, positively correlated with the dista

223 now only sparsely documented, namely longer intergenic regions, post-horizontal gene transfer (HGT)

224 H3K27me3 mark were more abundant (> 80%) in intergenic regions, whereas DBSs for H3K4me3 were distri

225 of 6mA reveals that this mark is enriched at intergenic regions, with a preference for certain superf

226 d burden of short deletions was primarily in intergenic regions.

227 g chromatin accessibility in gene bodies and intergenic regions.

228 DNMT3A and maintenance of DNA methylation at intergenic regions.

229 trand switch regions, telomeric regions, and intergenic regions.

230 gnition of DNA photoproducts, prevalently in intergenic regions.

231 1, DHRS12, ITPK1, ACSF3 and TNFRSF13C, and 2 intergenic regions.

232 ier microsatellite loci located in conserved intergenic regions.

233 hylation are localized to CpG islands within intergenic regions.

234 majority of detected heteroplasmies occur in intergenic regions.

235 -enhancers demonstrated extensive binding at intergenic regions.

236 tion start sites, within gene bodies, and in intergenic regions.

237 moters in gene bodies and non-coding RNAs in intergenic regions.

238 matin accessibility at a large subset of the intergenic regions.

239 GC-rich regions and located predominantly in intergenic regions.

240 promoters, coding exons, introns and distal intergenic regions.

241 rious genomic locations, including genic and intergenic regions.

242 ne expression by altering the copy number of intergenic regulatory regions.

243 These results suggest that pervasive intergenic repetitive sequence expression during human s

244 long noncoding RNA, Hox transcript antisense intergenic RNA (HOTAIR).

245 study, we report that HOTAIR (HOX antisense intergenic RNA) is upregulated in tamoxifen-resistant br

246 lncRNA) HOTAIR (for HOX Transcript Antisense Intergenic RNA) mediates a physical interaction between

247 ithin the NANCI (Nkx2.1-associated noncoding intergenic RNA)-Nkx2.1 gene duplex that is essential for

248 s of non-coding RNA including microRNA, long intergenic RNA, small nucleolar RNA, natural antisense t

249 Long intergenic RNAs (lincRNAs) play critical roles in eukary

250 unique expression of coding, noncoding, and intergenic RNAs in the mature mouse brain with RNA-Seq a

251 duction near genes compared with the rest of intergenic sequences is greater in a species with larger

252 ding alternative rbcS genes and adjoining 5'-intergenic sequences revealed that Rubisco production wa

253 utative mammary-specific enhancer within the intergenic sequences separating the two Stat5 genes.

254 ntiation, the preferred targets are intronic/intergenic sequences with enhancer-like activity.

255 actor and disengagement of RNA polymerase at intergenic sequences, particularly those at the NP:P and

256 r novel exons derived from both intronic and intergenic sequences.

257 RNAs that are transcribed from intronic and intergenic sequences.

258 An intergenic single-nucleotide polymorphism (rs4445257) on

259 here dI is the number of intergenic SNPs per intergenic site.

260 th of purifying selection operating over all intergenic sites is consistently intermediate between th

261 observed in addicted rats occurred mostly at intergenic sites located on long and short interspersed

262 vide these CTCF sites into three categories: intergenic sites remote from any coding element, upstrea

263 The results showed that one intergenic SNP (rs11901793), which is 20 kb upstream of

264 e an intronic SNP in FOXP1 at locus 3p13, an intergenic SNP at 3q28 near TP63, and an intergenic SNP

265 an intergenic SNP at 3q28 near TP63, and an intergenic SNP at 9p22 near BNC2.

266 identified 35 SNPs in 12 wheat genes and one intergenic SNP in the Sbwm1 region that showed a signifi

267 d the dI/dS ratio, where dI is the number of intergenic SNPs per intergenic site.

268 We find that intergenic SNPs tend to locate in distal OCRs, and our c

269 e a potential mechanism for trait-associated intergenic SNPs that may contribute to phenotypic variat

270 Despite 10-fold variation in intergenic space among species, the majority of open chr

271 that contained a transposon inserted in the intergenic space between sufC and sufD (sufD*), resultin

272 n to amplify a variable region of the 23S-5S intergenic spacer (IGS) ofRickettsiaspp.

273 We investigated the fungal intergenic spacer (IGS) sequence in combination with nan

274 Despite preserved intergenic spacer (IGS) structure, they showed altered c

275 nged in head-to-tail fashion separated by an intergenic spacer (IGS).

276 One large 101 bp intergenic spacer between trnY and cox1 was in S. varius

277 microsatellites loci (nSSRs) and three cpDNA intergenic spacer regions.

278 ing cytochrome oxidase gene subunit II - the intergenic spacer.

279 nucleic acid structures known as R-loops at intergenic spacers flanking nucleolar rRNA genes.

280 noncoding RNAs from the ribosomal DNA (rDNA) intergenic spacers, consistent with its previously repor

281 and notable improvements in the assembly of intergenic spaces and centromeres.

282 P2 and other latency-associated transcripts, intergenic splicing at the BZLF2 locus, and antisense tr

283 splicing sites, thus are likely products of 'intergenic splicing'.

284 xist at significantly lower frequencies than intergenic SVs.

285 tion sequence and expression conservation of intergenic transcribed regions (ITRs) in four Poaceae sp

286 ammatory conditions via the production of an intergenic transcript linking neuronal and immune Fpr ge

287 s of genomes has raised the question whether intergenic transcription represents the activity of nove

288 Within these domains, intergenic transcriptional enhancers evade heterochromat

289 nscripts and from DUX4-induced dsRNA-forming intergenic transcripts enriched for endogenous retroviru

290 alternative splice isoforms, and regulatory intergenic transcripts).

291 ll genomic regions including exons, introns, intergenic, TTS (transcription termination sites) and pr

292 n OPCML (P=9.89 x 10(-6)), and rs7700147, an intergenic variant (P=2.93 x 10(-5)).

293 , in LEP, ZNF800, KLHL31, and ACTL9, and one intergenic variant near KLF14.

294 authors discovered 2 novel AF variants, the intergenic variant rs72700114, between the genes LINC011

295 ocus and upstream of EMSY; EMSY, LRRC32, and intergenic variants all appear to be within a single top

296 ntronic variants, two 3' UTR variants and 23 intergenic variants.

297 Intergenic viral DNA fragments (less than 400 bp) contai

298 summary, we identified and characterized an intergenic VNTR polymorphism in S. pyogenes that affects

299 Here, we report an intergenic VNTR polymorphism that confers an altered lev

300 and silencing were used to identify a novel intergenic Y-linked lncRNA, named lnc-KDM5D-4, and inves