Variant report
Variant | rs9874263 |
---|---|
Chromosome Location | chr3:155760000-155760001 |
allele | C/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] |
---|---|
rs12330401 | 0.89[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs13058807 | 1.00[ASN][1000 genomes] |
rs13059614 | 1.00[ASN][1000 genomes] |
rs13062883 | 1.00[ASN][1000 genomes] |
rs13065118 | 1.00[ASN][1000 genomes] |
rs13069492 | 1.00[ASN][1000 genomes] |
rs13070956 | 1.00[ASN][1000 genomes] |
rs13074749 | 1.00[ASN][1000 genomes] |
rs13076854 | 1.00[ASN][1000 genomes] |
rs13077891 | 1.00[ASN][1000 genomes] |
rs13077893 | 1.00[ASN][1000 genomes] |
rs13085540 | 1.00[ASN][1000 genomes] |
rs13086158 | 1.00[ASN][1000 genomes] |
rs13086539 | 1.00[ASN][1000 genomes] |
rs13086888 | 1.00[ASN][1000 genomes] |
rs13092781 | 1.00[ASN][1000 genomes] |
rs13094737 | 1.00[ASN][1000 genomes] |
rs13098116 | 1.00[ASN][1000 genomes] |
rs13099875 | 1.00[ASN][1000 genomes] |
rs1499053 | 1.00[ASN][1000 genomes] |
rs16825721 | 1.00[ASN][1000 genomes] |
rs16825722 | 1.00[ASN][1000 genomes] |
rs2013676 | 1.00[ASN][1000 genomes] |
rs28454940 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28653682 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28670754 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs34176040 | 1.00[ASN][1000 genomes] |
rs34431563 | 1.00[ASN][1000 genomes] |
rs34447473 | 1.00[ASN][1000 genomes] |
rs34582489 | 1.00[ASN][1000 genomes] |
rs34611996 | 1.00[ASN][1000 genomes] |
rs34636155 | 1.00[ASN][1000 genomes] |
rs34721485 | 1.00[ASN][1000 genomes] |
rs34769075 | 1.00[ASN][1000 genomes] |
rs34786673 | 1.00[ASN][1000 genomes] |
rs34859273 | 1.00[ASN][1000 genomes] |
rs34908778 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs34965136 | 1.00[ASN][1000 genomes] |
rs34971897 | 1.00[ASN][1000 genomes] |
rs35081098 | 1.00[ASN][1000 genomes] |
rs35120330 | 1.00[ASN][1000 genomes] |
rs35306833 | 1.00[ASN][1000 genomes] |
rs35336094 | 1.00[ASN][1000 genomes] |
rs35385116 | 1.00[ASN][1000 genomes] |
rs35388604 | 1.00[ASN][1000 genomes] |
rs35692708 | 1.00[ASN][1000 genomes] |
rs35917295 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs35938711 | 1.00[ASN][1000 genomes] |
rs35972274 | 1.00[ASN][1000 genomes] |
rs36101183 | 1.00[ASN][1000 genomes] |
rs36106222 | 1.00[ASN][1000 genomes] |
rs36124391 | 1.00[ASN][1000 genomes] |
rs4378930 | 1.00[ASN][1000 genomes] |
rs55868315 | 1.00[ASN][1000 genomes] |
rs56000398 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs56213840 | 1.00[ASN][1000 genomes] |
rs57525215 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs58227176 | 1.00[ASN][1000 genomes] |
rs58487502 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs59289038 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6441048 | 1.00[ASN][1000 genomes] |
rs66496214 | 1.00[ASN][1000 genomes] |
rs66718940 | 1.00[ASN][1000 genomes] |
rs67049008 | 1.00[ASN][1000 genomes] |
rs67139403 | 1.00[ASN][1000 genomes] |
rs67148190 | 1.00[ASN][1000 genomes] |
rs67341546 | 1.00[ASN][1000 genomes] |
rs67420553 | 1.00[ASN][1000 genomes] |
rs67482406 | 1.00[ASN][1000 genomes] |
rs6767282 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6770125 | 1.00[ASN][1000 genomes] |
rs6775190 | 1.00[ASN][1000 genomes] |
rs67780510 | 1.00[ASN][1000 genomes] |
rs6781558 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs67899274 | 1.00[ASN][1000 genomes] |
rs67955446 | 1.00[ASN][1000 genomes] |
rs6805895 | 1.00[ASN][1000 genomes] |
rs68176279 | 1.00[ASN][1000 genomes] |
rs68188495 | 1.00[ASN][1000 genomes] |
rs71310462 | 1.00[ASN][1000 genomes] |
rs71310463 | 1.00[ASN][1000 genomes] |
rs71310465 | 1.00[ASN][1000 genomes] |
rs73159054 | 1.00[ASN][1000 genomes] |
rs73159063 | 1.00[ASN][1000 genomes] |
rs73159074 | 1.00[ASN][1000 genomes] |
rs73159092 | 1.00[ASN][1000 genomes] |
rs73161026 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73162706 | 1.00[ASN][1000 genomes] |
rs73873481 | 1.00[ASN][1000 genomes] |
rs7615287 | 1.00[ASN][1000 genomes] |
rs7615469 | 1.00[ASN][1000 genomes] |
rs7617514 | 1.00[ASN][1000 genomes] |
rs7617878 | 1.00[ASN][1000 genomes] |
rs7627181 | 1.00[ASN][1000 genomes] |
rs7627649 | 1.00[ASN][1000 genomes] |
rs7627831 | 1.00[ASN][1000 genomes] |
rs7639203 | 1.00[ASN][1000 genomes] |
rs7644218 | 0.80[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs7649451 | 1.00[ASN][1000 genomes] |
rs9683003 | 1.00[ASN][1000 genomes] |
rs9813738 | 0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9837458 | 0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9850516 | 0.94[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs9866512 | 0.89[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs9882341 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv592084 | chr3:155751484-155830578 | Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv521239 | chr3:155755327-155762725 | Weak transcription Enhancers Active TSS | TF binding regionCpG islandlncRNA | 1 gene(s) | inside rSNPs | diseases |
3 | nsv965225 | chr3:155758196-155767076 | Enhancers Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:155758000-155764800 | Weak transcription | Right Atrium | heart |
2 | chr3:155759800-155761000 | Enhancers | HepG2 | liver |