Variant report
Variant | rs17159589 |
---|---|
Chromosome Location | chr7:84692489-84692490 |
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] |
---|---|
rs10085820 | 1.00[AMR][1000 genomes] |
rs10216037 | 1.00[AMR][1000 genomes] |
rs10224192 | 1.00[AMR][1000 genomes] |
rs10226288 | 1.00[AMR][1000 genomes] |
rs10227790 | 1.00[AMR][1000 genomes] |
rs10229365 | 1.00[AMR][1000 genomes] |
rs10229476 | 1.00[AMR][1000 genomes] |
rs10229726 | 1.00[AMR][1000 genomes] |
rs10230012 | 1.00[AMR][1000 genomes] |
rs10230209 | 1.00[AMR][1000 genomes] |
rs10231169 | 1.00[AMR][1000 genomes] |
rs10231227 | 1.00[AMR][1000 genomes] |
rs10234337 | 1.00[AMR][1000 genomes] |
rs10235044 | 1.00[AMR][1000 genomes] |
rs10235804 | 1.00[AMR][1000 genomes] |
rs10238552 | 1.00[AMR][1000 genomes] |
rs10238803 | 1.00[AMR][1000 genomes] |
rs10239054 | 1.00[AMR][1000 genomes] |
rs10241357 | 1.00[AMR][1000 genomes] |
rs10242005 | 1.00[AMR][1000 genomes] |
rs10242855 | 1.00[AMR][1000 genomes] |
rs10243021 | 1.00[AMR][1000 genomes] |
rs10243755 | 1.00[AMR][1000 genomes] |
rs10243828 | 1.00[AMR][1000 genomes] |
rs10243859 | 1.00[AMR][1000 genomes] |
rs10247729 | 1.00[AMR][1000 genomes] |
rs10248781 | 1.00[AMR][1000 genomes] |
rs10249004 | 1.00[AMR][1000 genomes] |
rs10250111 | 1.00[AMR][1000 genomes] |
rs10252528 | 1.00[AMR][1000 genomes] |
rs10252836 | 1.00[AMR][1000 genomes] |
rs10253565 | 1.00[AMR][1000 genomes] |
rs10253650 | 1.00[AMR][1000 genomes] |
rs10254645 | 1.00[AMR][1000 genomes] |
rs10254905 | 1.00[AMR][1000 genomes] |
rs10256352 | 1.00[AMR][1000 genomes] |
rs10256709 | 1.00[AMR][1000 genomes] |
rs10256725 | 1.00[AMR][1000 genomes] |
rs10256947 | 1.00[AMR][1000 genomes] |
rs10257324 | 1.00[AMR][1000 genomes] |
rs10258219 | 1.00[AMR][1000 genomes] |
rs10258244 | 1.00[AMR][1000 genomes] |
rs10264103 | 1.00[AMR][1000 genomes] |
rs10268505 | 1.00[AMR][1000 genomes] |
rs10269671 | 1.00[AMR][1000 genomes] |
rs10271353 | 1.00[AMR][1000 genomes] |
rs10271605 | 1.00[AMR][1000 genomes] |
rs10273523 | 1.00[AMR][1000 genomes] |
rs10273534 | 1.00[AMR][1000 genomes] |
rs10273650 | 1.00[AMR][1000 genomes] |
rs10275794 | 1.00[AMR][1000 genomes] |
rs10277419 | 1.00[AMR][1000 genomes] |
rs10279991 | 1.00[AMR][1000 genomes] |
rs10282093 | 1.00[AMR][1000 genomes] |
rs12334236 | 1.00[AMR][1000 genomes] |
rs13438389 | 1.00[AMR][1000 genomes] |
rs1430595 | 1.00[AMR][1000 genomes] |
rs17148268 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17148271 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17159502 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17159553 | 1.00[AMR][1000 genomes] |
rs17159580 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17159590 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17159596 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17159599 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17159607 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs17159609 | 1.00[AMR][1000 genomes] |
rs1830384 | 1.00[AMR][1000 genomes] |
rs1830385 | 1.00[AMR][1000 genomes] |
rs1830386 | 1.00[AMR][1000 genomes] |
rs1835404 | 1.00[AMR][1000 genomes] |
rs1919288 | 1.00[AMR][1000 genomes] |
rs1919289 | 1.00[AMR][1000 genomes] |
rs2178116 | 1.00[AMR][1000 genomes] |
rs28366993 | 1.00[AMR][1000 genomes] |
rs28379695 | 1.00[AMR][1000 genomes] |
rs28395450 | 1.00[AMR][1000 genomes] |
rs28412718 | 1.00[AMR][1000 genomes] |
rs28428821 | 1.00[AMR][1000 genomes] |
rs28450350 | 1.00[AMR][1000 genomes] |
rs28451585 | 1.00[AMR][1000 genomes] |
rs28503172 | 1.00[AMR][1000 genomes] |
rs28576399 | 1.00[AMR][1000 genomes] |
rs28610512 | 1.00[AMR][1000 genomes] |
rs28618178 | 1.00[AMR][1000 genomes] |
rs28648964 | 1.00[AMR][1000 genomes] |
rs28667540 | 1.00[AMR][1000 genomes] |
rs28715185 | 1.00[AMR][1000 genomes] |
rs41518350 | 0.85[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs4398846 | 1.00[AMR][1000 genomes] |
rs57698546 | 1.00[AMR][1000 genomes] |
rs57948301 | 0.91[AFR][1000 genomes];1.00[AMR][1000 genomes] |
rs58279956 | 1.00[AMR][1000 genomes] |
rs59738022 | 0.86[AFR][1000 genomes] |
rs9655926 | 1.00[AMR][1000 genomes] |
rs9655927 | 1.00[AMR][1000 genomes] |
rs9886001 | 1.00[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949446 | chr7:84003501-84763823 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 20 gene(s) | inside rSNPs | diseases |
2 | esv2422324 | chr7:84530290-84944913 | Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive region | 7 gene(s) | inside rSNPs | diseases |
3 | nsv916645 | chr7:84678606-85420011 | Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
4 | nsv869255 | chr7:84678606-85444155 | Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | diseases |
5 | nsv1032610 | chr7:84683282-84725413 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh | TF binding regionChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:84656200-84694800 | Weak transcription | Fetal Stomach | stomach |
2 | chr7:84676400-84694800 | Weak transcription | Colon Smooth Muscle | Colon |
3 | chr7:84679200-84692600 | Weak transcription | H1 BMP4 Derived Mesendoderm Cultured Cells | ES cell derived |
4 | chr7:84680400-84694600 | Weak transcription | Fetal Kidney | kidney |
5 | chr7:84684000-84700000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr7:84684400-84695000 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
7 | chr7:84685800-84695600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
8 | chr7:84687400-84695200 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
9 | chr7:84691400-84693000 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
10 | chr7:84692400-84695000 | Weak transcription | Fetal Lung | lung |