Variant report
Variant | rs62271620 |
---|---|
Chromosome Location | chr3:110240514-110240515 |
allele | A/G |
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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rs_ID | r2[population] |
---|---|
rs1028026 | 0.81[ASN][1000 genomes] |
rs1028027 | 0.81[ASN][1000 genomes] |
rs10934045 | 0.84[ASN][1000 genomes] |
rs10934046 | 0.82[ASN][1000 genomes] |
rs10934063 | 0.89[EUR][1000 genomes] |
rs10934064 | 0.89[EUR][1000 genomes] |
rs12487462 | 0.82[ASN][1000 genomes] |
rs13062461 | 0.85[ASN][1000 genomes] |
rs1398346 | 0.88[ASN][1000 genomes] |
rs1398347 | 0.81[ASN][1000 genomes] |
rs1398348 | 0.82[ASN][1000 genomes] |
rs1398349 | 0.82[ASN][1000 genomes] |
rs1398354 | 0.82[ASN][1000 genomes] |
rs1398409 | 0.82[ASN][1000 genomes] |
rs1512514 | 0.80[ASN][1000 genomes] |
rs1512519 | 0.82[ASN][1000 genomes] |
rs1512540 | 0.84[ASN][1000 genomes] |
rs1512660 | 0.84[ASN][1000 genomes] |
rs1512661 | 0.84[ASN][1000 genomes] |
rs1512662 | 0.95[EUR][1000 genomes] |
rs1574700 | 0.84[ASN][1000 genomes] |
rs1606345 | 0.81[ASN][1000 genomes] |
rs1606346 | 0.81[ASN][1000 genomes] |
rs1606348 | 0.81[ASN][1000 genomes] |
rs1606349 | 0.82[ASN][1000 genomes] |
rs1606350 | 0.95[EUR][1000 genomes] |
rs16856946 | 0.89[EUR][1000 genomes] |
rs1849379 | 0.90[ASN][1000 genomes] |
rs1913088 | 0.84[ASN][1000 genomes] |
rs1913100 | 0.82[ASN][1000 genomes] |
rs2055966 | 0.81[ASN][1000 genomes] |
rs2055967 | 0.81[ASN][1000 genomes] |
rs2055968 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2399335 | 0.81[ASN][1000 genomes] |
rs2399336 | 0.82[ASN][1000 genomes] |
rs2399337 | 0.83[ASN][1000 genomes] |
rs2895375 | 0.95[EUR][1000 genomes] |
rs4682180 | 0.87[ASN][1000 genomes] |
rs4682181 | 0.81[ASN][1000 genomes] |
rs4682594 | 0.84[ASN][1000 genomes] |
rs56067719 | 0.84[ASN][1000 genomes] |
rs57198450 | 0.94[EUR][1000 genomes] |
rs57680282 | 1.00[EUR][1000 genomes] |
rs58500543 | 0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs59612531 | 0.94[EUR][1000 genomes] |
rs59985710 | 0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs60302938 | 0.89[EUR][1000 genomes] |
rs62270060 | 1.00[EUR][1000 genomes] |
rs62270063 | 1.00[EUR][1000 genomes] |
rs62270076 | 1.00[EUR][1000 genomes] |
rs62270083 | 1.00[EUR][1000 genomes] |
rs62270086 | 1.00[EUR][1000 genomes] |
rs62270095 | 1.00[EUR][1000 genomes] |
rs62270100 | 1.00[EUR][1000 genomes] |
rs62270121 | 0.89[EUR][1000 genomes] |
rs62270122 | 0.89[EUR][1000 genomes] |
rs62270123 | 0.89[EUR][1000 genomes] |
rs62270124 | 0.94[EUR][1000 genomes] |
rs62270127 | 0.89[EUR][1000 genomes] |
rs62270128 | 0.94[EUR][1000 genomes] |
rs62270130 | 0.89[EUR][1000 genomes] |
rs62270134 | 0.94[EUR][1000 genomes] |
rs62271562 | 0.84[EUR][1000 genomes] |
rs62271576 | 0.89[EUR][1000 genomes] |
rs62271578 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes] |
rs62271586 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs62271587 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs62271588 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs62271591 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs62271592 | 0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs62271606 | 1.00[EUR][1000 genomes] |
rs62271607 | 1.00[EUR][1000 genomes] |
rs62271608 | 1.00[EUR][1000 genomes] |
rs62271609 | 0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs62271610 | 1.00[EUR][1000 genomes] |
rs62271612 | 0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs62271615 | 0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs62271616 | 0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs62271618 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62271621 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs62271636 | 1.00[EUR][1000 genomes] |
rs62271639 | 1.00[EUR][1000 genomes] |
rs62271642 | 1.00[EUR][1000 genomes] |
rs62271644 | 1.00[EUR][1000 genomes] |
rs62271646 | 0.85[EUR][1000 genomes] |
rs62271647 | 1.00[EUR][1000 genomes] |
rs62271761 | 0.83[EUR][1000 genomes] |
rs62271763 | 0.89[EUR][1000 genomes] |
rs62271766 | 0.94[EUR][1000 genomes] |
rs6437914 | 0.89[AFR][1000 genomes];0.87[AMR][1000 genomes] |
rs67064864 | 0.80[ASN][1000 genomes] |
rs67166271 | 0.82[ASN][1000 genomes] |
rs6765569 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs6768474 | 0.81[EUR][1000 genomes] |
rs6772035 | 0.89[EUR][1000 genomes] |
rs6776067 | 0.89[EUR][1000 genomes] |
rs6781483 | 0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs6784648 | 0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs73217304 | 0.82[ASN][1000 genomes] |
rs73217311 | 0.81[ASN][1000 genomes] |
rs73217315 | 0.81[ASN][1000 genomes] |
rs7613348 | 0.84[ASN][1000 genomes] |
rs7616260 | 0.82[ASN][1000 genomes] |
rs7617903 | 0.84[EUR][1000 genomes] |
rs7627828 | 0.82[ASN][1000 genomes] |
rs7628733 | 0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7631316 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs7632974 | 0.89[EUR][1000 genomes] |
rs7634524 | 1.00[EUR][1000 genomes] |
rs7634536 | 0.84[EUR][1000 genomes] |
rs7638870 | 0.81[ASN][1000 genomes] |
rs7640587 | 0.84[ASN][1000 genomes] |
rs7640755 | 0.81[ASN][1000 genomes] |
rs7640794 | 0.84[ASN][1000 genomes] |
rs7644836 | 0.81[ASN][1000 genomes] |
rs7650722 | 0.89[EUR][1000 genomes] |
rs7652062 | 0.81[EUR][1000 genomes] |
rs7652124 | 0.81[ASN][1000 genomes] |
rs949970 | 0.80[ASN][1000 genomes] |
rs9653909 | 1.00[EUR][1000 genomes] |
rs9809100 | 0.81[ASN][1000 genomes] |
rs9809312 | 0.95[EUR][1000 genomes] |
rs9813893 | 0.81[ASN][1000 genomes] |
rs9814176 | 0.81[ASN][1000 genomes] |
rs9815066 | 0.81[ASN][1000 genomes] |
rs9815868 | 0.81[ASN][1000 genomes] |
rs9816249 | 0.81[ASN][1000 genomes] |
rs9820458 | 0.81[ASN][1000 genomes] |
rs9825259 | 0.89[EUR][1000 genomes] |
rs9826577 | 0.84[ASN][1000 genomes] |
rs9831873 | 0.88[ASN][1000 genomes] |
rs9839635 | 0.81[ASN][1000 genomes] |
rs9843950 | 0.81[ASN][1000 genomes] |
rs9846566 | 0.84[ASN][1000 genomes] |
rs9847279 | 0.81[ASN][1000 genomes] |
rs9858359 | 0.89[EUR][1000 genomes] |
rs9860708 | 0.84[ASN][1000 genomes] |
rs9867550 | 0.84[ASN][1000 genomes] |
rs9872133 | 0.90[ASN][1000 genomes] |
rs9872620 | 0.82[ASN][1000 genomes] |
rs9873714 | 0.89[EUR][1000 genomes] |
rs9877123 | 0.81[ASN][1000 genomes] |
rs9877235 | 0.88[ASN][1000 genomes] |
rs9877354 | 0.81[ASN][1000 genomes] |
rs9877472 | 0.84[ASN][1000 genomes] |
rs9877920 | 0.88[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv999414 | chr3:110103126-110340180 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
2 | nsv829670 | chr3:110134650-110308256 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv520365 | chr3:110155172-110441165 | Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv1001144 | chr3:110158316-110431113 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
5 | nsv536687 | chr3:110158316-110431113 | Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv1001810 | chr3:110158316-110522247 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
7 | nsv1010230 | chr3:110204439-110588814 | Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
8 | nsv536688 | chr3:110204439-110588814 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
9 | nsv829672 | chr3:110206693-110361632 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
10 | nsv1011034 | chr3:110209344-110559021 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
11 | nsv536689 | chr3:110209344-110559021 | Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:110232000-110245200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
2 | chr3:110239400-110240600 | Enhancers | NHDF-Ad | bronchial |
3 | chr3:110239400-110241000 | Enhancers | NHLF | lung |
4 | chr3:110239400-110241400 | Enhancers | HUVEC | blood vessel |
5 | chr3:110239600-110240600 | Enhancers | NH-A | brain |
6 | chr3:110239600-110240600 | Enhancers | Osteobl | bone |
7 | chr3:110239800-110240600 | Enhancers | Muscle Satellite Cultured Cells | -- |
8 | chr3:110240000-110245400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
9 | chr3:110240400-110240800 | Enhancers | K562 | blood |
10 | chr3:110240400-110245200 | Weak transcription | HMEC | breast |