Variant report
Variant | rs11045796 |
---|---|
Chromosome Location | chr12:21308623-21308624 |
allele | A/G |
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] |
---|---|
rs1002552 | 1.00[ASN][1000 genomes] |
rs10444413 | 1.00[ASW][hapmap];0.81[CEU][hapmap];1.00[ASN][1000 genomes] |
rs10841761 | 1.00[ASN][1000 genomes] |
rs10841766 | 1.00[ASN][1000 genomes] |
rs10841767 | 1.00[ASN][1000 genomes] |
rs10841768 | 1.00[ASN][1000 genomes] |
rs10841784 | 1.00[ASN][1000 genomes] |
rs10841789 | 1.00[ASN][1000 genomes] |
rs10841795 | 1.00[ASW][hapmap] |
rs11045642 | 1.00[ASN][1000 genomes] |
rs11045655 | 1.00[ASN][1000 genomes] |
rs11045657 | 1.00[CEU][hapmap];0.87[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045658 | 0.93[CEU][hapmap] |
rs11045680 | 1.00[CEU][hapmap] |
rs11045681 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[MEX][hapmap];0.82[TSI][hapmap] |
rs11045690 | 1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[TSI][hapmap] |
rs11045691 | 1.00[CEU][hapmap] |
rs11045694 | 1.00[CEU][hapmap] |
rs11045696 | 1.00[CEU][hapmap] |
rs11045699 | 1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045701 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045702 | 1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045703 | 1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045704 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045711 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045715 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045717 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045729 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045736 | 1.00[ASN][1000 genomes] |
rs11045737 | 1.00[AFR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045742 | 1.00[CEU][hapmap] |
rs11045771 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045772 | 0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045773 | 1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045780 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045781 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045783 | 0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045785 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045786 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045787 | 1.00[ASW][hapmap];1.00[CEU][hapmap];0.88[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];0.96[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045797 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045798 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045799 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045801 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045803 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045805 | 0.93[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045806 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045807 | 1.00[ASN][1000 genomes] |
rs11045813 | 1.00[ASN][1000 genomes] |
rs11045816 | 0.81[CEU][hapmap];1.00[ASN][1000 genomes] |
rs11045818 | 1.00[ASN][1000 genomes] |
rs11045819 | 1.00[ASN][1000 genomes] |
rs11045820 | 1.00[ASN][1000 genomes] |
rs11045821 | 1.00[ASN][1000 genomes] |
rs11045823 | 1.00[ASN][1000 genomes] |
rs11045824 | 1.00[ASW][hapmap];1.00[ASN][1000 genomes] |
rs11045825 | 1.00[ASN][1000 genomes] |
rs11045831 | 1.00[ASN][1000 genomes] |
rs11045832 | 1.00[ASN][1000 genomes] |
rs11045843 | 1.00[ASN][1000 genomes] |
rs11045856 | 1.00[ASN][1000 genomes] |
rs11045858 | 1.00[ASN][1000 genomes] |
rs11045862 | 1.00[ASN][1000 genomes] |
rs11045863 | 1.00[ASN][1000 genomes] |
rs11045870 | 1.00[ASN][1000 genomes] |
rs11045871 | 1.00[ASN][1000 genomes] |
rs11045872 | 1.00[ASN][1000 genomes] |
rs11045873 | 1.00[ASN][1000 genomes] |
rs11045874 | 1.00[ASN][1000 genomes] |
rs11045884 | 1.00[ASN][1000 genomes] |
rs11045887 | 1.00[ASN][1000 genomes] |
rs11045891 | 1.00[ASW][hapmap];1.00[ASN][1000 genomes] |
rs11045892 | 1.00[ASN][1000 genomes] |
rs11045893 | 1.00[ASN][1000 genomes] |
rs11045897 | 1.00[ASN][1000 genomes] |
rs11045916 | 1.00[ASN][1000 genomes] |
rs11045917 | 1.00[ASN][1000 genomes] |
rs11045918 | 1.00[ASW][hapmap];1.00[ASN][1000 genomes] |
rs11045928 | 1.00[ASN][1000 genomes] |
rs11045930 | 1.00[ASN][1000 genomes] |
rs11045942 | 1.00[ASN][1000 genomes] |
rs11045946 | 1.00[ASW][hapmap];1.00[ASN][1000 genomes] |
rs11045952 | 1.00[ASN][1000 genomes] |
rs11045953 | 1.00[ASN][1000 genomes] |
rs11045956 | 1.00[ASN][1000 genomes] |
rs11045957 | 1.00[ASW][hapmap];1.00[ASN][1000 genomes] |
rs11045958 | 1.00[ASN][1000 genomes] |
rs11045960 | 1.00[ASN][1000 genomes] |
rs11045961 | 1.00[ASW][hapmap];1.00[ASN][1000 genomes] |
rs11045972 | 1.00[ASN][1000 genomes] |
rs11045978 | 1.00[ASN][1000 genomes] |
rs11494712 | 0.93[CEU][hapmap] |
rs11494720 | 1.00[ASN][1000 genomes] |
rs11513224 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11513226 | 1.00[ASN][1000 genomes] |
rs11513228 | 1.00[ASN][1000 genomes] |
rs11513411 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11519266 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11522782 | 1.00[ASN][1000 genomes] |
rs12307908 | 1.00[ASN][1000 genomes] |
rs12311451 | 1.00[ASN][1000 genomes] |
rs12367829 | 1.00[ASN][1000 genomes] |
rs12368356 | 1.00[ASN][1000 genomes] |
rs12368481 | 1.00[ASN][1000 genomes] |
rs12370842 | 1.00[ASN][1000 genomes] |
rs12371160 | 0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12371390 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12371570 | 1.00[ASN][1000 genomes] |
rs12371691 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12372124 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12372260 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12372374 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12811381 | 1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12812279 | 1.00[ASN][1000 genomes] |
rs12814646 | 1.00[ASN][1000 genomes] |
rs12815795 | 1.00[ASN][1000 genomes] |
rs12819980 | 1.00[CEU][hapmap] |
rs12819994 | 1.00[ASN][1000 genomes] |
rs12820529 | 1.00[ASN][1000 genomes] |
rs12821068 | 1.00[ASN][1000 genomes] |
rs12821228 | 1.00[ASN][1000 genomes] |
rs12821721 | 1.00[ASN][1000 genomes] |
rs12826425 | 1.00[ASN][1000 genomes] |
rs12826495 | 1.00[CEU][hapmap] |
rs12827231 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12829704 | 1.00[ASN][1000 genomes] |
rs12830545 | 1.00[ASN][1000 genomes] |
rs1564367 | 1.00[ASN][1000 genomes] |
rs1564369 | 1.00[ASN][1000 genomes] |
rs17328763 | 1.00[ASW][hapmap];1.00[CEU][hapmap];0.88[GIH][hapmap];1.00[LWK][hapmap];0.85[MEX][hapmap];1.00[MKK][hapmap];0.93[TSI][hapmap];1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17329885 | 1.00[ASN][1000 genomes] |
rs17333533 | 1.00[ASW][hapmap] |
rs1910166 | 0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1910169 | 1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[MEX][hapmap];0.83[TSI][hapmap] |
rs2169969 | 1.00[ASN][1000 genomes] |
rs2199684 | 1.00[ASN][1000 genomes] |
rs2199686 | 1.00[ASN][1000 genomes] |
rs2417872 | 1.00[CEU][hapmap] |
rs2417972 | 1.00[ASN][1000 genomes] |
rs28802276 | 1.00[ASN][1000 genomes] |
rs2900480 | 1.00[ASN][1000 genomes] |
rs34022980 | 1.00[ASN][1000 genomes] |
rs34111581 | 1.00[ASN][1000 genomes] |
rs34211424 | 1.00[ASN][1000 genomes] |
rs34249976 | 1.00[ASN][1000 genomes] |
rs34632551 | 1.00[ASN][1000 genomes] |
rs34712739 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34888642 | 1.00[ASN][1000 genomes] |
rs35157563 | 1.00[ASN][1000 genomes] |
rs35236625 | 1.00[ASN][1000 genomes] |
rs35406304 | 1.00[ASN][1000 genomes] |
rs35428245 | 1.00[ASN][1000 genomes] |
rs35462387 | 1.00[ASN][1000 genomes] |
rs35642680 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35736956 | 1.00[ASN][1000 genomes] |
rs35901590 | 1.00[ASN][1000 genomes] |
rs35928112 | 1.00[ASN][1000 genomes] |
rs3794320 | 1.00[ASN][1000 genomes] |
rs4337089 | 1.00[ASW][hapmap];1.00[ASN][1000 genomes] |
rs4381410 | 1.00[ASN][1000 genomes] |
rs4442593 | 1.00[ASN][1000 genomes] |
rs55708035 | 1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs55720923 | 1.00[ASN][1000 genomes] |
rs55773124 | 1.00[ASN][1000 genomes] |
rs55820200 | 1.00[ASN][1000 genomes] |
rs56164184 | 1.00[ASN][1000 genomes] |
rs6487215 | 1.00[ASN][1000 genomes] |
rs66777941 | 1.00[ASN][1000 genomes] |
rs7137060 | 1.00[ASN][1000 genomes] |
rs71446755 | 1.00[ASN][1000 genomes] |
rs71446757 | 1.00[ASN][1000 genomes] |
rs71446760 | 1.00[ASN][1000 genomes] |
rs71446761 | 1.00[ASN][1000 genomes] |
rs71446762 | 1.00[ASN][1000 genomes] |
rs71446763 | 1.00[ASN][1000 genomes] |
rs7485550 | 1.00[ASN][1000 genomes] |
rs7956958 | 1.00[ASN][1000 genomes] |
rs7957158 | 1.00[ASN][1000 genomes] |
rs7957274 | 1.00[ASN][1000 genomes] |
rs7960384 | 1.00[ASN][1000 genomes] |
rs7960688 | 1.00[ASN][1000 genomes] |
rs7962263 | 1.00[ASN][1000 genomes] |
rs7962919 | 1.00[ASN][1000 genomes] |
rs7965059 | 1.00[ASN][1000 genomes] |
rs7967303 | 1.00[ASN][1000 genomes] |
rs7967403 | 1.00[ASN][1000 genomes] |
rs7977197 | 1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7978322 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1043890 | chr12:20659151-21309993 | Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 15 gene(s) | inside rSNPs | diseases |
2 | nsv541410 | chr12:20659151-21309993 | Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 15 gene(s) | inside rSNPs | diseases |
3 | nsv898872 | chr12:21000586-21413632 | Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv1045460 | chr12:21007732-21348247 | Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv1048648 | chr12:21007732-21410089 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv949142 | chr12:21008498-21382619 | Enhancers Active TSS Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
7 | nsv948700 | chr12:21008498-21422492 | Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
8 | nsv531958 | chr12:21008499-21377322 | ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
9 | nsv1039633 | chr12:21008519-21332904 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
10 | nsv1047113 | chr12:21008519-21402544 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
11 | nsv541411 | chr12:21008519-21402544 | ZNF genes & repeats Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
12 | nsv515735 | chr12:21010048-21420712 | Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
13 | nsv933139 | chr12:21011077-21404166 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
14 | nsv557710 | chr12:21011480-21404832 | Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
15 | nsv1038517 | chr12:21017375-21356781 | Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
16 | nsv541412 | chr12:21017375-21356781 | Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
17 | nsv1052893 | chr12:21017376-21356782 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
18 | nsv541413 | chr12:21017376-21356782 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
19 | nsv1051005 | chr12:21017575-21356642 | Genic enhancers Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
20 | nsv541414 | chr12:21017575-21356642 | Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
21 | nsv933316 | chr12:21017576-21404166 | ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
22 | nsv916519 | chr12:21017673-21356568 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
23 | nsv469159 | chr12:21124371-21404832 | Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
24 | nsv557717 | chr12:21124371-21404832 | Enhancers Strong transcription ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
25 | nsv1052587 | chr12:21149131-21420712 | Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
26 | nsv1050396 | chr12:21152478-21420712 | ZNF genes & repeats Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
27 | nsv1054132 | chr12:21165101-21402544 | Enhancers Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
28 | nsv541415 | chr12:21165101-21402544 | Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
29 | nsv933284 | chr12:21171894-21404166 | ZNF genes & repeats Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
30 | esv3439156 | chr12:21207396-21370189 | Genic enhancers Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
31 | nsv1041711 | chr12:21236384-21402544 | Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
32 | nsv1048033 | chr12:21267568-21336958 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
33 | nsv898880 | chr12:21282953-21321482 | Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG island | 1 gene(s) | inside rSNPs | diseases |
34 | nsv557719 | chr12:21291501-21316213 | Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS | n/a | n/a | inside rSNPs | diseases |
35 | esv1843766 | chr12:21291501-21317352 | Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS | n/a | n/a | inside rSNPs | diseases |
36 | nsv557720 | chr12:21292206-21315444 | Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS | n/a | n/a | inside rSNPs | diseases |
37 | nsv557721 | chr12:21294293-21315952 | Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription | n/a | n/a | inside rSNPs | diseases |
38 | nsv898881 | chr12:21294293-21317352 | Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription | n/a | n/a | inside rSNPs | diseases |
39 | nsv898882 | chr12:21294293-21321482 | Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS | n/a | n/a | inside rSNPs | diseases |
40 | nsv898883 | chr12:21294293-21450917 | Enhancers Active TSS Genic enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
41 | nsv557722 | chr12:21296344-21317922 | Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription | n/a | n/a | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:21308400-21309000 | Flanking Active TSS | Liver | Liver |
2 | chr12:21308600-21309000 | Enhancers | HUES48 Cell Line | embryonic stem cell |
3 | chr12:21308600-21309000 | Enhancers | iPS-15b Cell Line | embryonic stem cell |