Variant report
Variant | rs9638859 |
---|---|
Chromosome Location | chr7:3591333-3591334 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr7:3577804..3580555-chr7:3590884..3593146,2 | MCF-7 | breast: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10215541 | 0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10215554 | 0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs10215632 | 0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs10216009 | 0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10227151 | 0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10236989 | 0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10241070 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs10243981 | 0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs10264275 | 0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10272876 | 0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs10277776 | 0.82[ASN][1000 genomes] |
rs1114778 | 0.83[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs1114779 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1114780 | 0.88[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs11531491 | 0.85[AMR][1000 genomes] |
rs11531493 | 0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs12111969 | 0.94[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs12670592 | 0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs12672248 | 0.88[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1403160 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs1403161 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs1522505 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs1608136 | 0.88[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs16870870 | 0.88[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs17133420 | 0.82[AMR][1000 genomes] |
rs17133426 | 0.84[AMR][1000 genomes] |
rs17133432 | 0.84[AMR][1000 genomes] |
rs17133439 | 0.85[AMR][1000 genomes] |
rs17133445 | 0.85[AMR][1000 genomes] |
rs17133497 | 0.92[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs17133501 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs17133520 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs17133523 | 0.92[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs17133529 | 0.93[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs17133533 | 0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs17133535 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs17133554 | 0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17133555 | 0.96[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17133566 | 0.83[ASN][1000 genomes] |
rs1882427 | 0.87[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1882428 | 0.89[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1882429 | 0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes] |
rs1922017 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs1922019 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2141825 | 0.82[ASN][1000 genomes] |
rs2177168 | 0.84[AMR][1000 genomes] |
rs2178626 | 0.82[ASN][1000 genomes] |
rs2272526 | 0.88[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs2272527 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs28412607 | 0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs28451147 | 0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs28709062 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs28832366 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs35791987 | 0.86[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs4291167 | 0.94[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs4496870 | 0.85[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs5022333 | 0.89[AMR][1000 genomes] |
rs55878136 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs55933090 | 0.89[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs56134531 | 0.88[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs56234403 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs56341242 | 0.88[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs57462209 | 0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs57704507 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs57733415 | 0.83[AMR][1000 genomes] |
rs57743735 | 0.88[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs58028517 | 0.91[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs58601265 | 0.88[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs58748813 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs58979693 | 0.82[AMR][1000 genomes];0.80[EUR][1000 genomes] |
rs59228270 | 0.89[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs60268542 | 0.92[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs60867986 | 0.92[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs61605079 | 0.90[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs6462126 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs6462127 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs6462128 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs67253031 | 0.85[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs67540761 | 0.88[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs68004656 | 0.86[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs68143552 | 0.87[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs6947615 | 0.92[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs6962132 | 0.83[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs6966652 | 0.89[ASN][1000 genomes] |
rs73035954 | 0.85[AMR][1000 genomes];0.85[EUR][1000 genomes] |
rs73035962 | 0.91[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs73035977 | 0.91[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs73038556 | 0.84[AMR][1000 genomes] |
rs73293551 | 0.83[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs73671854 | 0.84[AMR][1000 genomes] |
rs7779462 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7780340 | 0.92[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7787559 | 0.84[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7789656 | 0.90[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs7791215 | 0.92[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7794992 | 0.92[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs7795323 | 0.90[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7805283 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs7805598 | 0.91[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs7808972 | 0.83[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs9639598 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs9654994 | 0.81[ASN][1000 genomes] |
rs9771445 | 0.92[AMR][1000 genomes];0.89[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1018173 | chr7:3258989-3879848 | Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
2 | nsv538660 | chr7:3258989-3879848 | Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 6 gene(s) | inside rSNPs | diseases |
3 | nsv1016555 | chr7:3298478-3872512 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
4 | nsv538661 | chr7:3298478-3872512 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
5 | esv2764026 | chr7:3365002-3618361 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
6 | nsv916071 | chr7:3423207-3697428 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
7 | nsv528715 | chr7:3451251-3598581 | Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive region | 3 gene(s) | inside rSNPs | diseases |
8 | nsv605902 | chr7:3464896-3598581 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
9 | nsv1034716 | chr7:3512406-3616155 | Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
10 | nsv887334 | chr7:3531275-3635105 | Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
11 | nsv1023888 | chr7:3539750-3638242 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
12 | nsv1034298 | chr7:3539750-3646251 | Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
13 | nsv1029264 | chr7:3549193-3622532 | Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
14 | nsv1032031 | chr7:3554760-3609584 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
15 | nsv538675 | chr7:3554760-3609584 | Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
16 | nsv464271 | chr7:3556132-3605340 | Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
17 | nsv605905 | chr7:3556132-3605340 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
18 | nsv1025623 | chr7:3558521-3606640 | Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
19 | nsv605906 | chr7:3559826-3605340 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
20 | nsv1027274 | chr7:3561252-3602457 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
21 | nsv538676 | chr7:3561252-3602457 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
22 | nsv1034671 | chr7:3565156-3607294 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
23 | nsv538677 | chr7:3565156-3607294 | Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
24 | nsv1028274 | chr7:3565356-3607155 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
25 | nsv538678 | chr7:3565356-3607155 | Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
26 | nsv830888 | chr7:3577214-3776276 | Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
27 | esv1840932 | chr7:3585560-3618827 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:3577600-3600200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr7:3578800-3593200 | Weak transcription | Aorta | Aorta |
3 | chr7:3586400-3593400 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
4 | chr7:3587600-3593000 | Weak transcription | H9 Cell Line | embryonic stem cell |
5 | chr7:3588800-3593000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
6 | chr7:3588800-3598000 | Weak transcription | Gastric | stomach |
7 | chr7:3589600-3592000 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
8 | chr7:3589800-3592000 | Weak transcription | iPS-15b Cell Line | embryonic stem cell |
9 | chr7:3589800-3593200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
10 | chr7:3590200-3592200 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
11 | chr7:3590200-3592400 | Weak transcription | H1 Cell Line | embryonic stem cell |
12 | chr7:3590200-3593200 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
13 | chr7:3590400-3593000 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
14 | chr7:3590800-3591400 | Enhancers | Fetal Lung | lung |
15 | chr7:3591200-3591400 | Enhancers | Pancreatic Islets | Pancreatic Islet |