Variant report
Variant | rs1669410 |
---|---|
Chromosome Location | chr12:11338559-11338560 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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Variant related genes | Relation type |
---|---|
ENSG00000256629 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11557132 | 0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1376742 | 0.83[ASN][1000 genomes] |
rs1451765 | 0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1451766 | 0.82[ASN][1000 genomes] |
rs1451772 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1451774 | 0.82[ASN][1000 genomes] |
rs1551191 | 1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1551192 | 0.83[ASN][1000 genomes] |
rs1650020 | 0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1650029 | 1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1650030 | 0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1650031 | 0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1650053 | 0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1669412 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1669414 | 0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1669418 | 0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1669422 | 0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs17817150 | 0.82[ASN][1000 genomes] |
rs1817104 | 0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1823663 | 0.83[ASN][1000 genomes] |
rs1823664 | 0.83[ASN][1000 genomes] |
rs1839859 | 0.83[ASN][1000 genomes] |
rs2008253 | 0.83[ASN][1000 genomes] |
rs2019629 | 0.83[ASN][1000 genomes] |
rs2019633 | 0.83[ASN][1000 genomes] |
rs2123006 | 0.95[ASN][1000 genomes] |
rs2123007 | 0.95[ASN][1000 genomes] |
rs2167481 | 0.95[ASN][1000 genomes] |
rs2218818 | 0.82[ASN][1000 genomes] |
rs2416544 | 0.95[ASN][1000 genomes] |
rs2416545 | 0.95[ASN][1000 genomes] |
rs2416546 | 0.95[ASN][1000 genomes] |
rs2416547 | 0.95[ASN][1000 genomes] |
rs2559581 | 0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs2597918 | 0.82[ASN][1000 genomes] |
rs2597919 | 0.83[ASN][1000 genomes] |
rs2597920 | 0.83[ASN][1000 genomes] |
rs2597921 | 0.83[ASN][1000 genomes] |
rs2597923 | 0.83[ASN][1000 genomes] |
rs2599396 | 0.83[ASN][1000 genomes] |
rs2599404 | 0.83[ASN][1000 genomes] |
rs2600350 | 0.82[ASN][1000 genomes] |
rs2600351 | 0.83[ASN][1000 genomes] |
rs2600352 | 0.83[ASN][1000 genomes] |
rs2600353 | 0.83[ASN][1000 genomes] |
rs2600354 | 0.83[ASN][1000 genomes] |
rs2600357 | 0.83[ASN][1000 genomes] |
rs2708331 | 0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2708368 | 0.82[ASN][1000 genomes] |
rs2708369 | 0.82[ASN][1000 genomes] |
rs2708370 | 0.83[ASN][1000 genomes] |
rs2923860 | 0.83[ASN][1000 genomes] |
rs319267 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs319268 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs319271 | 1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs319272 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs319273 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs319274 | 0.92[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs34000114 | 0.82[ASN][1000 genomes] |
rs34018339 | 0.95[ASN][1000 genomes] |
rs34082341 | 0.83[ASN][1000 genomes] |
rs34134804 | 0.82[ASN][1000 genomes] |
rs34241192 | 0.83[ASN][1000 genomes] |
rs34270405 | 1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs34272839 | 0.82[ASN][1000 genomes] |
rs34288418 | 0.83[ASN][1000 genomes] |
rs34327967 | 0.83[ASN][1000 genomes] |
rs34436598 | 0.83[ASN][1000 genomes] |
rs34531956 | 0.95[ASN][1000 genomes] |
rs34536990 | 0.83[ASN][1000 genomes] |
rs34548551 | 0.83[ASN][1000 genomes] |
rs34590962 | 1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs34648613 | 0.82[ASN][1000 genomes] |
rs34685506 | 0.83[ASN][1000 genomes] |
rs34769150 | 0.83[ASN][1000 genomes] |
rs34843817 | 0.83[ASN][1000 genomes] |
rs34927715 | 0.83[ASN][1000 genomes] |
rs34949195 | 0.82[ASN][1000 genomes] |
rs35017789 | 0.82[ASN][1000 genomes] |
rs35021653 | 0.83[ASN][1000 genomes] |
rs35119575 | 0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs35124606 | 0.83[ASN][1000 genomes] |
rs35151793 | 0.95[ASN][1000 genomes] |
rs35183723 | 0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs35280352 | 0.83[ASN][1000 genomes] |
rs35340812 | 0.83[ASN][1000 genomes] |
rs35499317 | 0.82[ASN][1000 genomes] |
rs35650731 | 0.82[ASN][1000 genomes] |
rs35699328 | 0.83[ASN][1000 genomes] |
rs35813024 | 0.83[ASN][1000 genomes] |
rs35856529 | 0.83[ASN][1000 genomes] |
rs35893804 | 0.83[ASN][1000 genomes] |
rs35969491 | 0.82[ASN][1000 genomes] |
rs36050405 | 0.83[ASN][1000 genomes] |
rs36062343 | 0.83[ASN][1000 genomes] |
rs36115011 | 0.83[ASN][1000 genomes] |
rs3863325 | 0.82[ASN][1000 genomes] |
rs3906996 | 0.83[ASN][1000 genomes] |
rs3911234 | 0.82[ASN][1000 genomes] |
rs3911800 | 0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs4101885 | 0.82[ASN][1000 genomes] |
rs4763638 | 1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs5020531 | 0.82[ASN][1000 genomes] |
rs61928449 | 0.82[ASN][1000 genomes] |
rs61928562 | 0.83[ASN][1000 genomes] |
rs61928564 | 0.83[ASN][1000 genomes] |
rs61928565 | 0.83[ASN][1000 genomes] |
rs61928566 | 0.83[ASN][1000 genomes] |
rs61928569 | 0.83[ASN][1000 genomes] |
rs61928595 | 0.83[ASN][1000 genomes] |
rs61928597 | 0.83[ASN][1000 genomes] |
rs61928602 | 0.83[ASN][1000 genomes] |
rs61928610 | 0.83[ASN][1000 genomes] |
rs61928618 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs61928619 | 0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs61928642 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs61928643 | 0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs61928644 | 0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs61928646 | 0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs61931266 | 0.82[ASN][1000 genomes] |
rs61931270 | 0.83[ASN][1000 genomes] |
rs61931274 | 0.83[ASN][1000 genomes] |
rs61931278 | 0.80[ASN][1000 genomes] |
rs61931279 | 0.82[ASN][1000 genomes] |
rs6488347 | 0.84[ASN][1000 genomes] |
rs6488348 | 0.84[ASN][1000 genomes] |
rs6488349 | 0.84[ASN][1000 genomes] |
rs6488350 | 0.84[ASN][1000 genomes] |
rs6488351 | 0.83[ASN][1000 genomes] |
rs6488355 | 0.83[ASN][1000 genomes] |
rs6488356 | 0.83[ASN][1000 genomes] |
rs6488357 | 0.82[ASN][1000 genomes] |
rs6488358 | 0.82[ASN][1000 genomes] |
rs67471783 | 0.82[ASN][1000 genomes] |
rs67955183 | 0.82[ASN][1000 genomes] |
rs7132674 | 0.82[ASN][1000 genomes] |
rs7136602 | 0.82[ASN][1000 genomes] |
rs71453440 | 0.82[ASN][1000 genomes] |
rs7298544 | 0.82[ASN][1000 genomes] |
rs7302010 | 0.83[ASN][1000 genomes] |
rs7302711 | 0.82[ASN][1000 genomes] |
rs7310047 | 0.83[ASN][1000 genomes] |
rs7313796 | 0.83[ASN][1000 genomes] |
rs7486717 | 0.83[ASN][1000 genomes] |
rs7955495 | 0.83[ASN][1000 genomes] |
rs7959320 | 0.83[ASN][1000 genomes] |
rs7960823 | 0.83[ASN][1000 genomes] |
rs7965506 | 0.83[ASN][1000 genomes] |
rs7969625 | 0.95[ASN][1000 genomes] |
rs7970225 | 0.81[ASN][1000 genomes] |
rs7973730 | 0.83[ASN][1000 genomes] |
rs7976211 | 0.83[ASN][1000 genomes] |
rs7976950 | 0.82[ASN][1000 genomes] |
rs8300 | 0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs977473 | 0.81[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv2758294 | chr12:10969620-11714921 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 52 gene(s) | inside rSNPs | diseases |
2 | esv2759879 | chr12:10969620-11714921 | Genic enhancers Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 52 gene(s) | inside rSNPs | diseases |
3 | nsv1038277 | chr12:11060978-11504091 | Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 40 gene(s) | inside rSNPs | diseases |
4 | nsv428272 | chr12:11069845-11714921 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 47 gene(s) | inside rSNPs | diseases |
5 | nsv898783 | chr12:11185236-11338781 | ZNF genes & repeats Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 26 gene(s) | inside rSNPs | diseases |
6 | nsv898784 | chr12:11188140-11341521 | Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
7 | nsv1050050 | chr12:11192046-11436359 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 31 gene(s) | inside rSNPs | diseases |
8 | nsv1053783 | chr12:11203509-11495584 | Weak transcription ZNF genes & repeats Genic enhancers Enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 32 gene(s) | inside rSNPs | diseases |
9 | esv1807067 | chr12:11214215-11568895 | Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 33 gene(s) | inside rSNPs | diseases |
10 | nsv8918 | chr12:11337700-11339877 | Weak transcription Enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:11326200-11338600 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
2 | chr12:11326400-11355600 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
3 | chr12:11328000-11338600 | Weak transcription | Primary Natural Killer cells fromperipheralblood | blood |
4 | chr12:11328800-11340400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
5 | chr12:11330600-11365400 | Weak transcription | Primary T cells from cord blood | blood |