Variant report
Variant | rs10071066 |
---|---|
Chromosome Location | chr5:115538662-115538663 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10037305 | 0.80[AMR][1000 genomes] |
rs10041334 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10052301 | 0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10054966 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10055145 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10056927 | 0.89[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs10056931 | 0.87[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10057003 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10057462 | 0.82[ASN][1000 genomes] |
rs10057513 | 0.82[ASN][1000 genomes] |
rs10058275 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10058707 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10059719 | 0.82[ASN][1000 genomes] |
rs10059969 | 0.82[ASN][1000 genomes] |
rs10059989 | 0.82[ASN][1000 genomes] |
rs10062295 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10068730 | 0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10069565 | 0.80[ASN][1000 genomes] |
rs10069865 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10069927 | 0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10071141 | 0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10071359 | 0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs10073157 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10073199 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10074746 | 0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs10076480 | 0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10076543 | 0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10076547 | 0.89[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10076548 | 0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10478285 | 0.90[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs10478286 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10478287 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10478291 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10478292 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs10900714 | 0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1113909 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs11951682 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11952310 | 0.90[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs11954350 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11955144 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11955906 | 0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11957382 | 0.82[ASN][1000 genomes] |
rs12522977 | 0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs13163088 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1396484 | 0.90[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs1396485 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs1396486 | 0.90[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs1508870 | 0.82[ASN][1000 genomes] |
rs1508873 | 0.81[ASN][1000 genomes] |
rs1541654 | 0.95[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1543952 | 0.82[ASN][1000 genomes] |
rs1567338 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1567339 | 0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1820053 | 0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1876675 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs1876676 | 0.90[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs2112569 | 0.80[AMR][1000 genomes] |
rs2136207 | 0.82[ASN][1000 genomes] |
rs2161321 | 0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2174996 | 0.82[ASN][1000 genomes] |
rs2218883 | 0.80[AMR][1000 genomes] |
rs2218884 | 0.80[AMR][1000 genomes] |
rs2416434 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs2416435 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2416436 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs28812579 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs3902887 | 0.85[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs4260709 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4301260 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4305671 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4484468 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4507525 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4513731 | 0.80[AMR][1000 genomes] |
rs4518445 | 0.89[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4593303 | 0.82[ASN][1000 genomes] |
rs4921067 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs4921069 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs4921072 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs4921076 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs4921078 | 0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs55854033 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs55975619 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs57096658 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs57609580 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs58414661 | 0.82[ASN][1000 genomes] |
rs59279546 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs59447269 | 0.82[ASN][1000 genomes] |
rs61334805 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs61402552 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs62384182 | 0.89[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs62384183 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs62384185 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs62384210 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62384234 | 0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs62385210 | 0.81[ASN][1000 genomes] |
rs62385211 | 0.82[ASN][1000 genomes] |
rs6594957 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6859670 | 0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6866514 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6866773 | 0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6878871 | 0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6879075 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6883424 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs6887275 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs73253250 | 0.82[ASN][1000 genomes] |
rs73257272 | 0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs73780896 | 0.90[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7448122 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7449449 | 0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7700647 | 0.89[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7700973 | 0.89[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs7701528 | 0.82[ASN][1000 genomes] |
rs7701751 | 0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7701837 | 0.82[ASN][1000 genomes] |
rs7702152 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7702975 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7703124 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7703661 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7704561 | 0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7706670 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7707191 | 0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7707320 | 0.82[ASN][1000 genomes] |
rs7709426 | 0.95[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7709439 | 0.82[ASN][1000 genomes] |
rs7709791 | 0.82[ASN][1000 genomes] |
rs7709844 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7716307 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7717931 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7718483 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7718843 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7719318 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7720518 | 0.90[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs7721510 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7721982 | 0.82[ASN][1000 genomes] |
rs7723648 | 0.94[AMR][1000 genomes];0.96[ASN][1000 genomes] |
rs7724448 | 0.82[ASN][1000 genomes] |
rs7725500 | 0.95[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7725803 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7727528 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7727695 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7727974 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs7730943 | 0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7734614 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7735094 | 0.90[AMR][1000 genomes];0.80[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs9326995 | 0.90[AMR][1000 genomes];0.91[ASN][1000 genomes] |
rs9326997 | 0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9686231 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9686686 | 0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9687350 | 0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs9942399 | 0.80[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv882736 | chr5:115254723-115552945 | Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
2 | nsv882737 | chr5:115263853-115552945 | Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
3 | esv34146 | chr5:115315944-115729919 | Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 29 gene(s) | inside rSNPs | diseases |
4 | nsv527320 | chr5:115382097-115573543 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
5 | esv2755349 | chr5:115384101-115733101 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 24 gene(s) | inside rSNPs | diseases |
6 | nsv1019972 | chr5:115386860-115563533 | Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
7 | nsv537869 | chr5:115386860-115563533 | Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 19 gene(s) | inside rSNPs | diseases |
8 | nsv1018861 | chr5:115397834-115563533 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
9 | nsv537870 | chr5:115397834-115563533 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
10 | nsv882739 | chr5:115471015-115552945 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
11 | nsv882740 | chr5:115482794-115540041 | Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
12 | nsv882741 | chr5:115484252-115552945 | Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
13 | nsv1032531 | chr5:115489694-115583800 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
14 | nsv882742 | chr5:115489770-115584159 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
15 | nsv1034069 | chr5:115490345-115563533 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
16 | nsv537873 | chr5:115490345-115563533 | Weak transcription Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
17 | nsv882743 | chr5:115501792-115634127 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
18 | nsv1023880 | chr5:115508328-115563533 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
19 | nsv537874 | chr5:115508328-115563533 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
20 | nsv1021381 | chr5:115509949-115568193 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
21 | esv2757133 | chr5:115515719-115543623 | Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
22 | esv2759371 | chr5:115515719-115543623 | Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
23 | nsv524812 | chr5:115517238-115584159 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
24 | nsv10745 | chr5:115519518-115541964 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
25 | nsv1028993 | chr5:115523717-115563533 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
26 | nsv537875 | chr5:115523717-115563533 | ZNF genes & repeats Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS | TF binding regionChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
27 | nsv1019540 | chr5:115526349-115610020 | Weak transcription ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
28 | nsv965515 | chr5:115526545-115546176 | Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
29 | esv2752058 | chr5:115533065-115605198 | Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
30 | nsv1016585 | chr5:115533065-115605455 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
31 | nsv1032799 | chr5:115533065-115609552 | Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
32 | nsv1016924 | chr5:115533065-115610020 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:115518800-115548000 | Weak transcription | Psoas Muscle | Psoas |
2 | chr5:115522600-115540200 | Weak transcription | Primary B cells from peripheral blood | blood |
3 | chr5:115525800-115560000 | Weak transcription | Left Ventricle | heart |
4 | chr5:115527800-115539000 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
5 | chr5:115527800-115543800 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
6 | chr5:115529000-115539200 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
7 | chr5:115537200-115559400 | Weak transcription | Primary B cells from cord blood | blood |
8 | chr5:115537400-115539600 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
9 | chr5:115537400-115545000 | Weak transcription | Primary T helper naive cells fromperipheralblood | blood |
10 | chr5:115537400-115560000 | Weak transcription | Primary T cells from cord blood | blood |
11 | chr5:115537600-115542400 | Weak transcription | Fetal Intestine Large | intestine |
12 | chr5:115537600-115560200 | Weak transcription | Primary hematopoietic stem cells | blood |