Variant report
Variant | rs7634781 |
---|---|
Chromosome Location | chr3:82226496-82226497 |
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] |
---|---|
rs11127754 | 0.82[EUR][1000 genomes] |
rs11127757 | 0.90[EUR][1000 genomes] |
rs11127758 | 0.84[EUR][1000 genomes] |
rs11916839 | 0.90[EUR][1000 genomes] |
rs11917347 | 0.86[EUR][1000 genomes] |
rs11918223 | 0.90[EUR][1000 genomes] |
rs11919912 | 0.93[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11922298 | 0.84[EUR][1000 genomes] |
rs11929553 | 0.82[EUR][1000 genomes] |
rs12630225 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs13059531 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs13088518 | 0.81[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs13088543 | 0.84[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs13314987 | 0.84[EUR][1000 genomes] |
rs13321907 | 0.84[EUR][1000 genomes] |
rs1534668 | 0.93[EUR][1000 genomes] |
rs17019551 | 0.86[EUR][1000 genomes] |
rs1919559 | 0.93[EUR][1000 genomes] |
rs2068211 | 0.82[EUR][1000 genomes] |
rs2141489 | 0.86[EUR][1000 genomes] |
rs2178315 | 0.86[EUR][1000 genomes] |
rs2178316 | 0.95[EUR][1000 genomes] |
rs28455989 | 0.84[EUR][1000 genomes] |
rs28475537 | 0.86[EUR][1000 genomes] |
rs28536106 | 0.86[EUR][1000 genomes] |
rs28561953 | 0.86[EUR][1000 genomes] |
rs28564625 | 0.86[EUR][1000 genomes] |
rs28683026 | 0.90[EUR][1000 genomes] |
rs4521254 | 0.84[EUR][1000 genomes] |
rs60509851 | 0.84[EUR][1000 genomes] |
rs60782263 | 0.86[EUR][1000 genomes] |
rs62265731 | 0.86[EUR][1000 genomes] |
rs62265755 | 0.90[EUR][1000 genomes] |
rs62265757 | 0.86[EUR][1000 genomes] |
rs62268572 | 0.86[EUR][1000 genomes] |
rs6419747 | 0.84[EUR][1000 genomes] |
rs6548789 | 0.84[EUR][1000 genomes] |
rs6548790 | 0.86[EUR][1000 genomes] |
rs6548793 | 0.90[EUR][1000 genomes] |
rs66870475 | 0.86[EUR][1000 genomes] |
rs6763269 | 0.86[EUR][1000 genomes] |
rs6767358 | 0.86[EUR][1000 genomes] |
rs6769852 | 0.84[EUR][1000 genomes] |
rs6773980 | 0.86[EUR][1000 genomes] |
rs6774064 | 0.86[EUR][1000 genomes] |
rs6774157 | 0.86[EUR][1000 genomes] |
rs6776655 | 0.86[EUR][1000 genomes] |
rs6778814 | 0.90[EUR][1000 genomes] |
rs6781140 | 0.90[EUR][1000 genomes] |
rs6805116 | 0.86[EUR][1000 genomes] |
rs7611244 | 0.86[EUR][1000 genomes] |
rs7611492 | 0.86[EUR][1000 genomes] |
rs7612452 | 0.82[EUR][1000 genomes] |
rs7614689 | 0.86[EUR][1000 genomes] |
rs7615354 | 0.84[EUR][1000 genomes] |
rs7619146 | 0.86[EUR][1000 genomes] |
rs7622355 | 0.86[EUR][1000 genomes] |
rs7623648 | 0.90[EUR][1000 genomes] |
rs7635092 | 0.90[EUR][1000 genomes] |
rs9309885 | 0.82[EUR][1000 genomes] |
rs9811625 | 0.90[EUR][1000 genomes] |
rs9812010 | 0.86[EUR][1000 genomes] |
rs9814587 | 0.86[EUR][1000 genomes] |
rs9815442 | 0.90[EUR][1000 genomes] |
rs9816690 | 0.86[EUR][1000 genomes] |
rs9817048 | 0.88[CEU][hapmap];1.00[YRI][hapmap];0.86[EUR][1000 genomes] |
rs9819290 | 0.86[EUR][1000 genomes] |
rs9820525 | 0.88[EUR][1000 genomes] |
rs9820687 | 0.90[EUR][1000 genomes] |
rs9821368 | 0.86[EUR][1000 genomes] |
rs9821506 | 0.90[EUR][1000 genomes] |
rs9821800 | 0.84[EUR][1000 genomes] |
rs9822483 | 0.90[EUR][1000 genomes] |
rs9831887 | 0.90[EUR][1000 genomes] |
rs9832377 | 0.86[EUR][1000 genomes] |
rs9834983 | 0.84[EUR][1000 genomes] |
rs9836048 | 0.86[EUR][1000 genomes] |
rs9838997 | 0.86[EUR][1000 genomes] |
rs9840948 | 0.84[EUR][1000 genomes] |
rs9843444 | 0.86[EUR][1000 genomes] |
rs9845227 | 0.86[EUR][1000 genomes] |
rs9848134 | 0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs9851363 | 0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs9853043 | 0.86[EUR][1000 genomes] |
rs9857313 | 0.90[EUR][1000 genomes] |
rs9857742 | 0.86[EUR][1000 genomes] |
rs9859766 | 0.90[EUR][1000 genomes] |
rs9863450 | 0.90[EUR][1000 genomes] |
rs9866029 | 0.82[EUR][1000 genomes] |
rs9866312 | 0.86[EUR][1000 genomes] |
rs9866476 | 0.90[EUR][1000 genomes] |
rs9867563 | 0.84[EUR][1000 genomes] |
rs9868182 | 0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs9869419 | 0.86[EUR][1000 genomes] |
rs9869718 | 0.84[EUR][1000 genomes] |
rs9872972 | 0.84[EUR][1000 genomes] |
rs9873073 | 0.86[EUR][1000 genomes] |
rs9875359 | 0.86[EUR][1000 genomes] |
rs9876062 | 0.84[EUR][1000 genomes] |
rs9876340 | 0.86[EUR][1000 genomes] |
rs9878115 | 0.86[EUR][1000 genomes] |
rs9878768 | 0.86[EUR][1000 genomes] |
rs9882486 | 0.86[EUR][1000 genomes] |
rs9882687 | 0.86[EUR][1000 genomes] |
rs9883163 | 0.90[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1007167 | chr3:82050178-82301466 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv877041 | chr3:82074024-82363196 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv1008429 | chr3:82089650-82510536 | Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
4 | nsv432460 | chr3:82107110-82508010 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
5 | nsv1005262 | chr3:82165228-82258781 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats | Chromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv1013820 | chr3:82175705-82968181 | Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
7 | nsv877043 | chr3:82198467-82311711 | Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS | lncRNA | 4 gene(s) | inside rSNPs | diseases |
8 | nsv877044 | chr3:82214617-82266033 | Enhancers Weak transcription ZNF genes & repeats | lncRNA | 4 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:82226400-82228000 | Enhancers | Ovary | ovary |