Variant report
Variant | rs59132771 |
---|---|
Chromosome Location | chr6:128621456-128621457 |
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] |
---|---|
rs11753971 | 1.00[ASN][1000 genomes] |
rs11964875 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11965122 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11965141 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11966128 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1339189 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1339196 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1416517 | 0.89[EUR][1000 genomes] |
rs1538498 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1612415 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055287 | 1.00[ASN][1000 genomes] |
rs17055307 | 1.00[ASN][1000 genomes] |
rs17055313 | 1.00[ASN][1000 genomes] |
rs17055324 | 1.00[ASN][1000 genomes] |
rs17055328 | 1.00[ASN][1000 genomes] |
rs17055339 | 1.00[ASN][1000 genomes] |
rs17055340 | 1.00[ASN][1000 genomes] |
rs17055343 | 1.00[ASN][1000 genomes] |
rs17055348 | 1.00[ASN][1000 genomes] |
rs17055350 | 1.00[ASN][1000 genomes] |
rs17055352 | 1.00[ASN][1000 genomes] |
rs17055362 | 1.00[ASN][1000 genomes] |
rs17055368 | 1.00[ASN][1000 genomes] |
rs17055373 | 1.00[ASN][1000 genomes] |
rs17055386 | 1.00[ASN][1000 genomes] |
rs17055450 | 1.00[ASN][1000 genomes] |
rs17055452 | 1.00[ASN][1000 genomes] |
rs17055554 | 1.00[ASN][1000 genomes] |
rs17055564 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055574 | 1.00[EUR][1000 genomes] |
rs17055596 | 1.00[EUR][1000 genomes] |
rs17055597 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055601 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055604 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055608 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055611 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055612 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055616 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055617 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055618 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055619 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055628 | 0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055630 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17055679 | 1.00[EUR][1000 genomes] |
rs17055689 | 0.91[EUR][1000 genomes] |
rs17055706 | 0.91[EUR][1000 genomes] |
rs17055717 | 0.89[EUR][1000 genomes] |
rs17055719 | 1.00[EUR][1000 genomes] |
rs17055727 | 0.89[EUR][1000 genomes] |
rs17055733 | 0.91[EUR][1000 genomes] |
rs17343887 | 1.00[EUR][1000 genomes] |
rs17350133 | 1.00[ASN][1000 genomes] |
rs17350286 | 1.00[ASN][1000 genomes] |
rs17353545 | 0.89[EUR][1000 genomes] |
rs17430131 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17430452 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17456343 | 1.00[EUR][1000 genomes] |
rs17456385 | 1.00[EUR][1000 genomes] |
rs17456601 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1768347 | 1.00[ASN][1000 genomes] |
rs1768353 | 1.00[ASN][1000 genomes] |
rs1768357 | 1.00[ASN][1000 genomes] |
rs1768360 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2027311 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4267969 | 1.00[EUR][1000 genomes] |
rs4466261 | 0.98[EUR][1000 genomes] |
rs55700986 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs55969073 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs56095177 | 0.94[EUR][1000 genomes] |
rs56241890 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs57318936 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs60915390 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6420738 | 0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6913718 | 0.98[EUR][1000 genomes] |
rs6931769 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6933821 | 0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72967021 | 0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72967026 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72967039 | 1.00[EUR][1000 genomes] |
rs72967046 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72967053 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72967056 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72967058 | 1.00[EUR][1000 genomes] |
rs72967074 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72967078 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72967081 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72967087 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72967090 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969051 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969054 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969059 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969061 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969063 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969067 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969070 | 1.00[EUR][1000 genomes] |
rs72969074 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969075 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969078 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969081 | 0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969088 | 0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969090 | 0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969093 | 0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969097 | 1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72969098 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72971103 | 1.00[EUR][1000 genomes] |
rs72971104 | 0.91[EUR][1000 genomes] |
rs72972078 | 0.91[EUR][1000 genomes] |
rs72972082 | 1.00[EUR][1000 genomes] |
rs72972084 | 1.00[EUR][1000 genomes] |
rs72972086 | 1.00[EUR][1000 genomes] |
rs72972090 | 0.89[EUR][1000 genomes] |
rs72972091 | 0.91[EUR][1000 genomes] |
rs73588649 | 1.00[ASN][1000 genomes] |
rs73588653 | 1.00[ASN][1000 genomes] |
rs73588664 | 1.00[ASN][1000 genomes] |
rs73588693 | 1.00[ASN][1000 genomes] |
rs73592692 | 1.00[ASN][1000 genomes] |
rs7759340 | 1.00[ASN][1000 genomes] |
rs7771630 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7773248 | 0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7776405 | 1.00[EUR][1000 genomes] |
rs9321114 | 0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9375562 | 0.86[EUR][1000 genomes] |
rs9402035 | 0.94[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1033443 | chr6:128306654-128899203 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
2 | nsv538440 | chr6:128306654-128899203 | Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 8 gene(s) | inside rSNPs | diseases |
3 | nsv886649 | chr6:128399657-128808054 | Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 4 gene(s) | inside rSNPs | diseases |
4 | nsv1020071 | chr6:128579774-129048919 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 15 gene(s) | inside rSNPs | diseases |
5 | nsv538441 | chr6:128579774-129048919 | Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 15 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:128593000-128631600 | Weak transcription | Left Ventricle | heart |
2 | chr6:128596800-128623600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr6:128597800-128625000 | Weak transcription | HSMM | muscle |
4 | chr6:128602400-128632400 | Weak transcription | Pancreas | Pancrea |
5 | chr6:128603000-128642800 | Weak transcription | Fetal Intestine Large | intestine |
6 | chr6:128604400-128630600 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
7 | chr6:128604400-128633200 | Weak transcription | Fetal Thymus | thymus |
8 | chr6:128605800-128627400 | Weak transcription | Bone Marrow Derived Cultured Mesenchymal Stem Cells | Bone marrow |
9 | chr6:128605800-128631200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
10 | chr6:128606200-128630600 | Weak transcription | Fetal Heart | heart |
11 | chr6:128609000-128646000 | Weak transcription | NH-A | brain |
12 | chr6:128610800-128643200 | Weak transcription | NHEK | skin |
13 | chr6:128612800-128630400 | Weak transcription | Brain Hippocampus Middle | brain |
14 | chr6:128613200-128640800 | Weak transcription | HepG2 | liver |
15 | chr6:128614200-128624000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
16 | chr6:128621400-128621600 | Strong transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |