Variant report
Variant | rs62469813 |
---|---|
Chromosome Location | chr7:117779652-117779653 |
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] |
---|---|
rs10265770 | 0.94[EUR][1000 genomes] |
rs12154543 | 0.94[EUR][1000 genomes] |
rs12155479 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12216555 | 0.94[EUR][1000 genomes] |
rs1468666 | 0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs16870173 | 0.94[EUR][1000 genomes] |
rs17140937 | 0.82[EUR][1000 genomes] |
rs17140943 | 0.82[EUR][1000 genomes] |
rs17141022 | 0.94[EUR][1000 genomes] |
rs17141033 | 0.94[EUR][1000 genomes] |
rs1990454 | 0.82[EUR][1000 genomes] |
rs2191921 | 0.94[EUR][1000 genomes] |
rs2191922 | 0.94[EUR][1000 genomes] |
rs2286855 | 0.94[EUR][1000 genomes] |
rs2286856 | 0.88[EUR][1000 genomes] |
rs2286857 | 0.94[EUR][1000 genomes] |
rs2286861 | 0.94[EUR][1000 genomes] |
rs2286862 | 0.94[EUR][1000 genomes] |
rs2286864 | 0.82[EUR][1000 genomes] |
rs3757799 | 0.94[EUR][1000 genomes] |
rs3757801 | 0.94[EUR][1000 genomes] |
rs3808172 | 0.94[EUR][1000 genomes] |
rs3808175 | 0.94[EUR][1000 genomes] |
rs3808178 | 0.94[EUR][1000 genomes] |
rs3808179 | 0.94[EUR][1000 genomes] |
rs3898536 | 0.91[EUR][1000 genomes] |
rs41281099 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4141029 | 0.94[EUR][1000 genomes] |
rs4141030 | 0.94[EUR][1000 genomes] |
rs62466461 | 0.94[EUR][1000 genomes] |
rs62466462 | 0.94[EUR][1000 genomes] |
rs62466463 | 0.94[EUR][1000 genomes] |
rs62466464 | 0.94[EUR][1000 genomes] |
rs62466466 | 0.94[EUR][1000 genomes] |
rs62466467 | 0.94[EUR][1000 genomes] |
rs62466468 | 0.94[EUR][1000 genomes] |
rs62466469 | 0.84[EUR][1000 genomes] |
rs62466472 | 0.88[EUR][1000 genomes] |
rs62466473 | 0.94[EUR][1000 genomes] |
rs62466474 | 0.94[EUR][1000 genomes] |
rs62466475 | 0.94[EUR][1000 genomes] |
rs62466476 | 0.94[EUR][1000 genomes] |
rs62466478 | 0.94[EUR][1000 genomes] |
rs62466512 | 0.94[EUR][1000 genomes] |
rs62466513 | 0.94[EUR][1000 genomes] |
rs62466514 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62466516 | 0.94[EUR][1000 genomes] |
rs62466517 | 0.94[EUR][1000 genomes] |
rs62466518 | 0.94[EUR][1000 genomes] |
rs62466519 | 0.94[EUR][1000 genomes] |
rs62466520 | 0.94[EUR][1000 genomes] |
rs62466521 | 0.94[EUR][1000 genomes] |
rs62466522 | 0.94[EUR][1000 genomes] |
rs62466523 | 0.94[EUR][1000 genomes] |
rs62466525 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62466526 | 0.94[EUR][1000 genomes] |
rs62466527 | 0.94[EUR][1000 genomes] |
rs62466528 | 0.94[EUR][1000 genomes] |
rs62466529 | 0.94[EUR][1000 genomes] |
rs62466531 | 0.94[EUR][1000 genomes] |
rs62466532 | 0.94[EUR][1000 genomes] |
rs62466533 | 0.94[EUR][1000 genomes] |
rs62466554 | 0.97[EUR][1000 genomes] |
rs62466555 | 0.94[EUR][1000 genomes] |
rs62466558 | 0.94[EUR][1000 genomes] |
rs62467931 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62467933 | 0.82[EUR][1000 genomes] |
rs62468165 | 0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62468169 | 0.94[EUR][1000 genomes] |
rs62468170 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62468171 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62468172 | 1.00[EUR][1000 genomes] |
rs62468173 | 0.81[EUR][1000 genomes] |
rs62468208 | 0.88[EUR][1000 genomes] |
rs62468210 | 0.82[EUR][1000 genomes] |
rs62468289 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62468290 | 0.82[EUR][1000 genomes] |
rs62468291 | 0.82[EUR][1000 genomes] |
rs62468292 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62468293 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62468294 | 0.94[EUR][1000 genomes] |
rs62468298 | 0.94[EUR][1000 genomes] |
rs62468299 | 0.94[EUR][1000 genomes] |
rs62468300 | 0.94[EUR][1000 genomes] |
rs62468301 | 0.94[EUR][1000 genomes] |
rs62468302 | 0.94[EUR][1000 genomes] |
rs62468303 | 0.94[EUR][1000 genomes] |
rs62468304 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62468305 | 0.94[EUR][1000 genomes] |
rs62468306 | 0.94[EUR][1000 genomes] |
rs62468307 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62468308 | 0.94[EUR][1000 genomes] |
rs62468309 | 0.94[EUR][1000 genomes] |
rs62468310 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62468311 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62468312 | 0.91[EUR][1000 genomes] |
rs62468313 | 0.91[EUR][1000 genomes] |
rs62468314 | 0.94[EUR][1000 genomes] |
rs62468315 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs62469766 | 0.97[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs62469768 | 0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62469784 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62469785 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62469787 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62469804 | 0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62469805 | 0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62469807 | 0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62469815 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6466651 | 0.94[EUR][1000 genomes] |
rs6942561 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6943182 | 0.94[EUR][1000 genomes] |
rs6945543 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs6946385 | 0.94[EUR][1000 genomes] |
rs6953131 | 0.94[EUR][1000 genomes] |
rs6955534 | 0.94[EUR][1000 genomes] |
rs6957412 | 0.94[EUR][1000 genomes] |
rs6957623 | 0.94[EUR][1000 genomes] |
rs6962486 | 0.94[EUR][1000 genomes] |
rs6964881 | 0.94[EUR][1000 genomes] |
rs6966522 | 0.86[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs6966654 | 0.97[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs6968077 | 0.82[EUR][1000 genomes] |
rs6971712 | 0.82[EUR][1000 genomes] |
rs6976656 | 0.94[EUR][1000 genomes] |
rs6980163 | 0.94[EUR][1000 genomes] |
rs7778155 | 0.80[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs7779197 | 0.82[EUR][1000 genomes] |
rs7779284 | 0.83[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs7779452 | 0.94[EUR][1000 genomes] |
rs7779944 | 0.82[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs7780322 | 0.81[AMR][1000 genomes];0.82[EUR][1000 genomes] |
rs7785444 | 1.00[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7792078 | 0.94[EUR][1000 genomes] |
rs7792264 | 0.94[EUR][1000 genomes] |
rs7792296 | 0.94[EUR][1000 genomes] |
rs7792510 | 0.94[EUR][1000 genomes] |
rs7792843 | 0.94[EUR][1000 genomes] |
rs7795737 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7796775 | 0.94[EUR][1000 genomes] |
rs7798307 | 0.82[EUR][1000 genomes] |
rs7798370 | 0.82[EUR][1000 genomes] |
rs7798529 | 0.94[EUR][1000 genomes] |
rs7804943 | 0.82[EUR][1000 genomes] |
rs7805538 | 0.82[EUR][1000 genomes] |
rs7805843 | 0.82[EUR][1000 genomes] |
rs7806876 | 0.94[EUR][1000 genomes] |
rs7807306 | 0.94[EUR][1000 genomes] |
rs7809247 | 0.94[EUR][1000 genomes] |
rs7809742 | 0.82[EUR][1000 genomes] |
rs7811055 | 0.82[EUR][1000 genomes] |
rs979651 | 0.88[EUR][1000 genomes] |
rs979653 | 0.94[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869971 | chr7:117420583-118274149 | Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 40 gene(s) | inside rSNPs | diseases |
2 | esv2752146 | chr7:117739049-117792049 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
3 | nsv1016264 | chr7:117739146-117792988 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
4 | esv2761358 | chr7:117739158-117793000 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv608260 | chr7:117739400-117792838 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | nsv1028064 | chr7:117740164-117792988 | Enhancers Flanking Active TSS Weak transcription | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
7 | nsv889088 | chr7:117744660-117913648 | Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
8 | esv3428352 | chr7:117754050-117783524 | Enhancers Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
9 | esv33380 | chr7:117768471-117793477 | Weak transcription Enhancers Flanking Active TSS | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:117779600-117792200 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |