Variant report
Variant | rs2707883 |
---|---|
Chromosome Location | chr7:79485590-79485591 |
allele | G/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] |
---|---|
rs1008311 | 0.94[ASN][1000 genomes] |
rs1009198 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1009199 | 0.94[ASN][1000 genomes] |
rs10229737 | 0.88[EUR][1000 genomes] |
rs10256778 | 0.97[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10486911 | 0.91[ASN][1000 genomes] |
rs10486912 | 0.87[ASN][1000 genomes] |
rs11974696 | 0.97[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11975054 | 0.94[ASN][1000 genomes] |
rs11975127 | 0.94[ASN][1000 genomes] |
rs12112783 | 0.91[ASN][1000 genomes] |
rs12113482 | 0.94[ASN][1000 genomes] |
rs12113913 | 0.93[ASN][1000 genomes] |
rs12155353 | 0.91[EUR][1000 genomes] |
rs12531185 | 0.94[ASN][1000 genomes] |
rs1293091 | 0.86[ASN][1000 genomes] |
rs1293109 | 0.86[ASN][1000 genomes] |
rs1293110 | 0.85[ASN][1000 genomes] |
rs1293111 | 0.84[ASN][1000 genomes] |
rs1293112 | 0.86[ASN][1000 genomes] |
rs1293113 | 0.86[ASN][1000 genomes] |
rs1293115 | 0.86[ASN][1000 genomes] |
rs1297413 | 0.86[ASN][1000 genomes] |
rs1319297 | 0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs16886703 | 0.85[ASN][1000 genomes] |
rs16886704 | 0.85[ASN][1000 genomes] |
rs17152926 | 0.81[ASN][1000 genomes] |
rs17152972 | 0.94[ASN][1000 genomes] |
rs17152982 | 0.91[ASN][1000 genomes] |
rs17152992 | 0.91[ASN][1000 genomes] |
rs17153038 | 0.90[ASN][1000 genomes] |
rs17153067 | 0.87[ASN][1000 genomes] |
rs17153072 | 0.87[ASN][1000 genomes] |
rs17153087 | 0.85[ASN][1000 genomes] |
rs17153094 | 0.85[ASN][1000 genomes] |
rs17793556 | 0.94[ASN][1000 genomes] |
rs1859196 | 0.89[EUR][1000 genomes] |
rs1922725 | 0.86[ASN][1000 genomes] |
rs1922726 | 0.81[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1922728 | 0.85[ASN][1000 genomes] |
rs1922731 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs1985747 | 0.91[ASN][1000 genomes] |
rs1985821 | 0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2107408 | 0.91[ASN][1000 genomes] |
rs2214430 | 0.97[EUR][1000 genomes] |
rs2246996 | 0.85[ASN][1000 genomes] |
rs2428627 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2525815 | 0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2525816 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2525820 | 0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2525822 | 0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2525825 | 0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2525826 | 0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2525827 | 0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs2525835 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2707858 | 0.84[ASN][1000 genomes] |
rs2707882 | 0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2707886 | 0.86[ASN][1000 genomes] |
rs2707887 | 0.86[ASN][1000 genomes] |
rs2707896 | 0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2707911 | 0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2707920 | 0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2707922 | 0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs2714653 | 0.86[ASN][1000 genomes] |
rs2714655 | 0.86[ASN][1000 genomes] |
rs2714656 | 0.85[ASN][1000 genomes] |
rs2714661 | 0.85[ASN][1000 genomes] |
rs2714662 | 0.86[ASN][1000 genomes] |
rs2714664 | 0.85[ASN][1000 genomes] |
rs2714695 | 0.83[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs2714696 | 0.81[AFR][1000 genomes];0.86[ASN][1000 genomes] |
rs333209 | 0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs333210 | 0.85[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs333211 | 0.90[ASN][1000 genomes] |
rs4352782 | 0.86[ASN][1000 genomes] |
rs4394329 | 0.81[ASN][1000 genomes] |
rs4460297 | 0.86[ASN][1000 genomes] |
rs57609264 | 0.94[ASN][1000 genomes] |
rs58237209 | 0.86[ASN][1000 genomes] |
rs59333025 | 0.85[ASN][1000 genomes] |
rs60424611 | 0.91[ASN][1000 genomes] |
rs61366591 | 0.94[ASN][1000 genomes] |
rs6466823 | 0.94[ASN][1000 genomes] |
rs6944276 | 0.85[ASN][1000 genomes] |
rs6946316 | 0.94[ASN][1000 genomes] |
rs6946466 | 0.89[EUR][1000 genomes] |
rs6947975 | 0.85[ASN][1000 genomes] |
rs6949163 | 0.94[ASN][1000 genomes] |
rs6949761 | 0.91[ASN][1000 genomes] |
rs6956324 | 0.85[ASN][1000 genomes] |
rs6957059 | 0.90[ASN][1000 genomes] |
rs6957093 | 0.90[ASN][1000 genomes] |
rs724336 | 0.87[ASN][1000 genomes] |
rs73368688 | 0.91[ASN][1000 genomes] |
rs73368692 | 0.91[ASN][1000 genomes] |
rs73370544 | 0.90[ASN][1000 genomes] |
rs73370545 | 0.90[ASN][1000 genomes] |
rs73370570 | 0.87[ASN][1000 genomes] |
rs73707160 | 0.94[ASN][1000 genomes] |
rs73709915 | 0.94[ASN][1000 genomes] |
rs73709922 | 0.90[ASN][1000 genomes] |
rs757191 | 0.88[EUR][1000 genomes] |
rs7777781 | 0.84[ASN][1000 genomes] |
rs7803517 | 0.97[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs7803852 | 0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs886475 | 0.85[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs981490 | 0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv888522 | chr7:79402551-79619012 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
2 | nsv5808 | chr7:79453632-79502455 | Enhancers Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:79484600-79485600 | Enhancers | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |