Variant report
Variant | rs779030 |
---|---|
Chromosome Location | chr3:21956627-21956628 |
allele | A/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] |
---|---|
rs10433570 | 0.94[ASN][1000 genomes] |
rs10440125 | 0.88[EUR][1000 genomes] |
rs10510521 | 0.94[ASN][1000 genomes] |
rs10865774 | 0.93[ASN][1000 genomes] |
rs10865775 | 0.90[ASN][1000 genomes] |
rs10865776 | 0.93[ASN][1000 genomes] |
rs10865777 | 0.93[ASN][1000 genomes] |
rs10865778 | 0.93[ASN][1000 genomes] |
rs10865779 | 0.81[ASN][1000 genomes] |
rs11129029 | 0.94[ASN][1000 genomes] |
rs1120052 | 0.91[ASN][1000 genomes] |
rs11706252 | 0.90[CEU][hapmap];0.85[CHB][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11714007 | 0.93[ASN][1000 genomes] |
rs11717781 | 0.82[ASN][1000 genomes] |
rs12330142 | 0.81[ASN][1000 genomes] |
rs12487611 | 0.93[ASN][1000 genomes] |
rs12487653 | 0.93[ASN][1000 genomes] |
rs12489286 | 0.88[ASN][1000 genomes] |
rs12490987 | 0.94[ASN][1000 genomes] |
rs12491046 | 0.93[ASN][1000 genomes] |
rs12493892 | 0.93[ASN][1000 genomes] |
rs12496539 | 0.91[ASN][1000 genomes] |
rs12638980 | 0.88[EUR][1000 genomes] |
rs13061226 | 0.90[CEU][hapmap];0.85[CHB][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs13066816 | 0.81[ASN][1000 genomes] |
rs13072115 | 0.91[ASN][1000 genomes] |
rs13076554 | 0.90[ASN][1000 genomes] |
rs13077139 | 0.91[ASN][1000 genomes] |
rs13078547 | 0.90[ASN][1000 genomes] |
rs13091957 | 0.91[ASN][1000 genomes] |
rs13091998 | 0.91[ASN][1000 genomes] |
rs13092149 | 0.91[ASN][1000 genomes] |
rs13092430 | 0.91[ASN][1000 genomes] |
rs13095013 | 0.90[EUR][1000 genomes] |
rs13096987 | 0.91[ASN][1000 genomes] |
rs13097724 | 0.90[ASN][1000 genomes] |
rs13097840 | 0.90[ASN][1000 genomes] |
rs1351323 | 0.93[ASN][1000 genomes] |
rs1383073 | 0.88[EUR][1000 genomes] |
rs1391330 | 0.94[CEU][hapmap];0.85[CHB][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1391331 | 0.88[CEU][hapmap];0.83[CHB][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1479961 | 0.94[ASN][1000 genomes] |
rs1479962 | 0.90[EUR][1000 genomes] |
rs1479963 | 0.88[EUR][1000 genomes] |
rs1479964 | 0.88[EUR][1000 genomes] |
rs1479965 | 0.90[EUR][1000 genomes] |
rs1479966 | 0.90[CEU][hapmap];0.81[CHB][hapmap] |
rs1479967 | 0.94[ASN][1000 genomes] |
rs1479968 | 0.90[CEU][hapmap];0.85[CHB][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1479969 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1479986 | 0.93[ASN][1000 genomes] |
rs1479987 | 0.93[ASN][1000 genomes] |
rs1479988 | 0.93[ASN][1000 genomes] |
rs1479989 | 0.93[ASN][1000 genomes] |
rs1486332 | 0.81[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1486333 | 0.89[CEU][hapmap];0.85[CHB][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1486372 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1497925 | 0.81[ASN][1000 genomes] |
rs1497938 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1497939 | 0.88[EUR][1000 genomes] |
rs1553085 | 0.86[ASN][1000 genomes] |
rs1564411 | 0.93[ASN][1000 genomes] |
rs1626065 | 0.80[ASN][1000 genomes] |
rs1684495 | 0.90[CEU][hapmap];0.85[CHB][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1694015 | 0.81[ASN][1000 genomes] |
rs1694042 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs17010120 | 0.94[ASN][1000 genomes] |
rs17010126 | 0.94[ASN][1000 genomes] |
rs17010229 | 0.93[ASN][1000 genomes] |
rs17010304 | 0.83[ASN][1000 genomes] |
rs17010418 | 0.80[ASN][1000 genomes] |
rs1842308 | 0.90[EUR][1000 genomes] |
rs1842309 | 0.90[EUR][1000 genomes] |
rs1843634 | 0.81[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs1846165 | 0.87[EUR][1000 genomes] |
rs1846166 | 0.90[CEU][hapmap];0.84[CHB][hapmap];0.88[EUR][1000 genomes] |
rs2061938 | 0.81[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2061939 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs2061940 | 0.81[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2593314 | 0.81[ASN][1000 genomes] |
rs2593325 | 0.80[ASN][1000 genomes] |
rs259482 | 0.90[ASN][1000 genomes] |
rs259508 | 0.87[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs259509 | 0.87[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs259510 | 0.86[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs259511 | 0.95[ASN][1000 genomes] |
rs259513 | 0.87[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs259514 | 0.93[ASN][1000 genomes] |
rs259515 | 0.93[ASN][1000 genomes] |
rs259517 | 0.93[ASN][1000 genomes] |
rs259518 | 0.93[ASN][1000 genomes] |
rs259520 | 0.93[ASN][1000 genomes] |
rs259521 | 0.92[ASN][1000 genomes] |
rs259537 | 0.87[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs259538 | 0.87[AMR][1000 genomes];0.97[ASN][1000 genomes] |
rs2620536 | 0.84[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes] |
rs34164902 | 0.94[ASN][1000 genomes] |
rs34598190 | 0.90[ASN][1000 genomes] |
rs34708854 | 0.86[ASN][1000 genomes] |
rs34718882 | 0.91[ASN][1000 genomes] |
rs34756955 | 0.89[ASN][1000 genomes] |
rs34815085 | 0.88[ASN][1000 genomes] |
rs34904582 | 0.91[ASN][1000 genomes] |
rs35338441 | 0.91[ASN][1000 genomes] |
rs35478822 | 0.81[ASN][1000 genomes] |
rs35541916 | 0.81[ASN][1000 genomes] |
rs35976399 | 0.90[ASN][1000 genomes] |
rs35993195 | 0.88[ASN][1000 genomes] |
rs36015330 | 0.91[ASN][1000 genomes] |
rs3821386 | 0.88[EUR][1000 genomes] |
rs3821388 | 0.88[EUR][1000 genomes] |
rs3821389 | 0.90[EUR][1000 genomes] |
rs3821390 | 0.88[EUR][1000 genomes] |
rs3821392 | 0.89[EUR][1000 genomes] |
rs3821393 | 0.87[EUR][1000 genomes] |
rs3821394 | 0.89[EUR][1000 genomes] |
rs4094000 | 0.93[ASN][1000 genomes] |
rs4270525 | 0.87[ASN][1000 genomes] |
rs4271936 | 0.80[ASN][1000 genomes] |
rs4348015 | 0.89[CEU][hapmap];0.84[CHB][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs4350938 | 0.94[ASN][1000 genomes] |
rs4355303 | 0.92[ASN][1000 genomes] |
rs4370048 | 0.93[ASN][1000 genomes] |
rs4420894 | 0.81[ASN][1000 genomes] |
rs4440143 | 0.80[ASN][1000 genomes] |
rs4610243 | 0.81[ASN][1000 genomes] |
rs4610244 | 0.81[ASN][1000 genomes] |
rs472117 | 0.84[CEU][hapmap];0.90[CHB][hapmap];0.81[ASN][1000 genomes] |
rs473395 | 0.81[ASN][1000 genomes] |
rs474387 | 0.84[CEU][hapmap];0.89[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes] |
rs476982 | 0.86[ASN][1000 genomes] |
rs478011 | 0.86[ASN][1000 genomes] |
rs478832 | 0.84[CEU][hapmap];0.90[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes] |
rs479923 | 0.83[ASN][1000 genomes] |
rs485483 | 0.84[CEU][hapmap];0.90[CHB][hapmap] |
rs485569 | 0.83[CEU][hapmap];0.90[CHB][hapmap];0.80[ASN][1000 genomes] |
rs4858370 | 0.87[AMR][1000 genomes];0.95[ASN][1000 genomes] |
rs500881 | 0.81[ASN][1000 genomes] |
rs501056 | 0.80[ASN][1000 genomes] |
rs502259 | 0.80[ASN][1000 genomes] |
rs503119 | 0.80[ASN][1000 genomes] |
rs504039 | 0.86[CEU][hapmap];0.85[ASN][1000 genomes] |
rs504757 | 0.90[ASN][1000 genomes] |
rs504917 | 0.81[ASN][1000 genomes] |
rs509513 | 0.84[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes] |
rs521724 | 0.84[ASN][1000 genomes] |
rs536133 | 0.81[ASN][1000 genomes] |
rs536196 | 0.81[ASN][1000 genomes] |
rs536986 | 0.85[ASN][1000 genomes] |
rs537870 | 0.83[ASN][1000 genomes] |
rs549089 | 0.82[ASN][1000 genomes] |
rs559082 | 0.80[ASN][1000 genomes] |
rs559861 | 0.80[ASN][1000 genomes] |
rs559894 | 0.81[ASN][1000 genomes] |
rs563648 | 0.80[ASN][1000 genomes] |
rs568153 | 0.84[ASN][1000 genomes] |
rs581184 | 0.81[ASN][1000 genomes] |
rs610316 | 0.85[ASN][1000 genomes] |
rs610320 | 0.85[ASN][1000 genomes] |
rs611146 | 0.87[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes] |
rs611545 | 0.84[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes] |
rs613768 | 0.81[ASN][1000 genomes] |
rs615095 | 0.81[ASN][1000 genomes] |
rs618682 | 0.80[ASN][1000 genomes] |
rs625615 | 0.84[CEU][hapmap];0.84[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes] |
rs627323 | 0.83[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes] |
rs627773 | 0.84[ASN][1000 genomes] |
rs627776 | 0.80[ASN][1000 genomes] |
rs628155 | 0.80[ASN][1000 genomes] |
rs628226 | 0.82[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes] |
rs629944 | 0.84[CEU][hapmap];0.89[CHB][hapmap] |
rs630299 | 0.89[CHB][hapmap] |
rs630769 | 0.84[CEU][hapmap];0.90[CHB][hapmap];0.81[ASN][1000 genomes] |
rs631246 | 0.83[CEU][hapmap];0.90[CHB][hapmap];0.81[ASN][1000 genomes] |
rs632070 | 0.83[CEU][hapmap];0.89[CHB][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes] |
rs638809 | 0.83[CEU][hapmap];0.89[CHB][hapmap];0.86[JPT][hapmap];0.83[ASN][1000 genomes] |
rs638844 | 0.83[CEU][hapmap];0.90[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes] |
rs641517 | 0.86[ASN][1000 genomes] |
rs641518 | 0.81[ASN][1000 genomes] |
rs641910 | 0.81[ASN][1000 genomes] |
rs642045 | 0.86[ASN][1000 genomes] |
rs645017 | 0.81[ASN][1000 genomes] |
rs6550633 | 0.89[CHB][hapmap];0.91[JPT][hapmap];0.84[ASN][1000 genomes] |
rs662789 | 0.81[ASN][1000 genomes] |
rs66575668 | 0.91[ASN][1000 genomes] |
rs67108462 | 0.94[ASN][1000 genomes] |
rs671377 | 0.84[ASN][1000 genomes] |
rs67326109 | 0.94[ASN][1000 genomes] |
rs680685 | 0.90[ASN][1000 genomes] |
rs7430341 | 0.93[ASN][1000 genomes] |
rs7433115 | 0.85[EUR][1000 genomes] |
rs7623923 | 0.91[ASN][1000 genomes] |
rs7628630 | 0.83[ASN][1000 genomes] |
rs7635217 | 0.91[ASN][1000 genomes] |
rs7635489 | 0.94[ASN][1000 genomes] |
rs7635497 | 0.94[ASN][1000 genomes] |
rs7636487 | 0.94[ASN][1000 genomes] |
rs7639658 | 0.80[ASN][1000 genomes] |
rs7645483 | 0.90[ASN][1000 genomes] |
rs7646871 | 0.94[ASN][1000 genomes] |
rs7646883 | 0.94[ASN][1000 genomes] |
rs7646975 | 0.94[ASN][1000 genomes] |
rs779029 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs8179942 | 0.93[ASN][1000 genomes] |
rs8179943 | 0.93[ASN][1000 genomes] |
rs8180016 | 0.93[ASN][1000 genomes] |
rs8180026 | 0.93[ASN][1000 genomes] |
rs8180049 | 0.93[ASN][1000 genomes] |
rs9809089 | 0.84[CEU][hapmap];0.84[CHB][hapmap];0.88[EUR][1000 genomes] |
rs9809324 | 0.85[CEU][hapmap];0.83[CHB][hapmap];0.88[EUR][1000 genomes] |
rs9810225 | 0.88[EUR][1000 genomes] |
rs9811248 | 0.94[CEU][hapmap];0.84[CHB][hapmap];0.86[EUR][1000 genomes] |
rs9811419 | 0.83[CHB][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs9814232 | 0.83[AMR][1000 genomes];0.90[ASN][1000 genomes] |
rs9816540 | 0.81[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs9821571 | 0.89[EUR][1000 genomes] |
rs9821707 | 0.89[EUR][1000 genomes] |
rs9821722 | 0.89[EUR][1000 genomes] |
rs9821912 | 0.89[EUR][1000 genomes] |
rs9822011 | 0.89[EUR][1000 genomes] |
rs9828376 | 0.88[EUR][1000 genomes] |
rs9828689 | 0.86[EUR][1000 genomes] |
rs9834671 | 0.88[EUR][1000 genomes] |
rs9841763 | 0.89[EUR][1000 genomes] |
rs9849994 | 0.82[ASN][1000 genomes] |
rs9854012 | 0.81[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs9854895 | 0.83[ASN][1000 genomes] |
rs9859150 | 0.89[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes] |
rs9859355 | 0.89[EUR][1000 genomes] |
rs9870712 | 0.81[ASN][1000 genomes] |
rs9873106 | 0.89[EUR][1000 genomes] |
rs9873232 | 0.89[EUR][1000 genomes] |
rs9879603 | 0.87[EUR][1000 genomes] |
rs9879858 | 0.93[CEU][hapmap];0.87[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv534005 | chr3:21387588-22003293 | Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 8 gene(s) | inside rSNPs | diseases |
2 | esv2751992 | chr3:21786893-22212357 | Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv948555 | chr3:21786893-22212357 | Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
4 | nsv834632 | chr3:21803941-21974082 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv1003085 | chr3:21887971-22415107 | Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv834633 | chr3:21918264-22088338 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
7 | nsv876614 | chr3:21919039-21994022 | Enhancers Weak transcription Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
8 | nsv998906 | chr3:21921707-21962293 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | n/a |
9 | nsv1014821 | chr3:21929218-21962293 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
10 | nsv876615 | chr3:21941259-21965999 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | n/a |
11 | nsv876616 | chr3:21946847-22310622 | Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Strong transcription Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
12 | nsv876617 | chr3:21955784-22310622 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr3:21953800-21956800 | Enhancers | Fetal Lung | lung |
2 | chr3:21954400-21960800 | Weak transcription | Placenta Amnion | Placenta Amnion |
3 | chr3:21954800-21957000 | Enhancers | Pancreatic Islets | Pancreatic Islet |
4 | chr3:21955400-21960600 | Weak transcription | NH-A | brain |
5 | chr3:21955600-21960600 | Weak transcription | Fetal Stomach | stomach |
6 | chr3:21955600-21960800 | Weak transcription | NHLF | lung |
7 | chr3:21955800-21961200 | Weak transcription | Mesenchymal Stem Cell Derived Adipocyte Cultured Cells | ES cell derived |
8 | chr3:21956200-21960600 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
9 | chr3:21956400-21960800 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
10 | chr3:21956400-21960800 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
11 | chr3:21956600-21960400 | Weak transcription | Muscle Satellite Cultured Cells | -- |
12 | chr3:21956600-21960400 | Weak transcription | NHDF-Ad | bronchial |