Variant report
Variant | rs55773124 |
---|---|
Chromosome Location | chr12:21397957-21397958 |
allele | A/C |
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[ASN][1000 genomes] |
rs10841761 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10841766 | 0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10841767 | 0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10841768 | 0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10841784 | 1.00[ASN][1000 genomes] |
rs10841789 | 1.00[ASN][1000 genomes] |
rs10841795 | 1.00[ASN][1000 genomes] |
rs11045729 | 1.00[ASN][1000 genomes] |
rs11045736 | 1.00[ASN][1000 genomes] |
rs11045737 | 1.00[ASN][1000 genomes] |
rs11045771 | 1.00[ASN][1000 genomes] |
rs11045772 | 1.00[ASN][1000 genomes] |
rs11045773 | 1.00[ASN][1000 genomes] |
rs11045780 | 1.00[ASN][1000 genomes] |
rs11045781 | 1.00[ASN][1000 genomes] |
rs11045783 | 1.00[ASN][1000 genomes] |
rs11045785 | 1.00[ASN][1000 genomes] |
rs11045786 | 1.00[ASN][1000 genomes] |
rs11045787 | 1.00[ASN][1000 genomes] |
rs11045796 | 1.00[ASN][1000 genomes] |
rs11045797 | 1.00[ASN][1000 genomes] |
rs11045798 | 1.00[ASN][1000 genomes] |
rs11045799 | 1.00[ASN][1000 genomes] |
rs11045801 | 1.00[ASN][1000 genomes] |
rs11045803 | 1.00[ASN][1000 genomes] |
rs11045805 | 1.00[ASN][1000 genomes] |
rs11045806 | 1.00[ASN][1000 genomes] |
rs11045807 | 1.00[ASN][1000 genomes] |
rs11045813 | 1.00[ASN][1000 genomes] |
rs11045816 | 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[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 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045863 | 0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045870 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045871 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045872 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045873 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045874 | 0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045884 | 0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045887 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045891 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045892 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045893 | 0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045897 | 0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11045916 | 1.00[ASN][1000 genomes] |
rs11045917 | 1.00[ASN][1000 genomes] |
rs11045918 | 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[ASN][1000 genomes] |
rs11045952 | 1.00[ASN][1000 genomes] |
rs11045953 | 1.00[ASN][1000 genomes] |
rs11045956 | 1.00[ASN][1000 genomes] |
rs11045957 | 1.00[ASN][1000 genomes] |
rs11045958 | 1.00[ASN][1000 genomes] |
rs11045960 | 1.00[ASN][1000 genomes] |
rs11045961 | 1.00[ASN][1000 genomes] |
rs11045972 | 1.00[ASN][1000 genomes] |
rs11045978 | 1.00[ASN][1000 genomes] |
rs11045981 | 1.00[ASN][1000 genomes] |
rs11494720 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11513224 | 1.00[ASN][1000 genomes] |
rs11513226 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11513228 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11513411 | 1.00[ASN][1000 genomes] |
rs11522782 | 1.00[ASN][1000 genomes] |
rs12307908 | 1.00[ASN][1000 genomes] |
rs12311451 | 0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12366994 | 0.83[EUR][1000 genomes] |
rs12367829 | 1.00[ASN][1000 genomes] |
rs12368356 | 1.00[ASN][1000 genomes] |
rs12368481 | 1.00[ASN][1000 genomes] |
rs12370842 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12371160 | 1.00[ASN][1000 genomes] |
rs12371570 | 1.00[ASN][1000 genomes] |
rs12371691 | 1.00[ASN][1000 genomes] |
rs12372124 | 1.00[ASN][1000 genomes] |
rs12372260 | 1.00[ASN][1000 genomes] |
rs12812279 | 1.00[ASN][1000 genomes] |
rs12814646 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12815795 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
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] |
rs12829704 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12830545 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1564367 | 1.00[ASN][1000 genomes] |
rs1564369 | 1.00[ASN][1000 genomes] |
rs17328763 | 1.00[ASN][1000 genomes] |
rs17329885 | 1.00[ASN][1000 genomes] |
rs2169969 | 1.00[ASN][1000 genomes] |
rs2199684 | 1.00[ASN][1000 genomes] |
rs2199686 | 1.00[ASN][1000 genomes] |
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 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];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[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] |
rs35462387 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35642680 | 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[ASN][1000 genomes] |
rs4381410 | 1.00[ASN][1000 genomes] |
rs4442593 | 1.00[ASN][1000 genomes] |
rs55708035 | 1.00[ASN][1000 genomes] |
rs55720923 | 1.00[ASN][1000 genomes] |
rs55820200 | 1.00[ASN][1000 genomes] |
rs56164184 | 0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6487215 | 1.00[ASN][1000 genomes] |
rs66777941 | 1.00[ASN][1000 genomes] |
rs7137060 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71446755 | 1.00[ASN][1000 genomes] |
rs71446757 | 1.00[ASN][1000 genomes] |
rs71446760 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71446761 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71446762 | 0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71446763 | 1.00[ASN][1000 genomes] |
rs7485550 | 1.00[ASN][1000 genomes] |
rs7957274 | 1.00[ASN][1000 genomes] |
rs7960384 | 0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7960688 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];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[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 | 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 |
2 | 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 |
3 | 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 |
4 | 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 |
5 | 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 |
6 | 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 |
7 | 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 |
8 | 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 |
9 | 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 |
10 | 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 |
11 | 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 |
12 | 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 |
13 | 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 |
14 | 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 |
15 | 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 |
16 | 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 |
17 | 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 |
18 | 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 |
19 | nsv898885 | chr12:21352541-21416413 | Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
20 | nsv898886 | chr12:21354494-21450250 | Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
21 | nsv898887 | chr12:21355537-21416413 | Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
22 | nsv898888 | chr12:21355537-21426087 | Strong transcription Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
23 | nsv1044200 | chr12:21357815-21410089 | Weak transcription Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
24 | nsv983239 | chr12:21392756-21405241 | Weak transcription Enhancers Strong transcription ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
25 | esv3390939 | chr12:21393734-21418537 | Enhancers Weak transcription Strong transcription ZNF genes & repeats | n/a | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:21397800-21399000 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |