Variant report
Variant | rs11691687 |
---|---|
Chromosome Location | chr2:186440524-186440525 |
allele | A/C |
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] |
---|---|
rs10170781 | 0.84[EUR][1000 genomes] |
rs10177147 | 0.84[EUR][1000 genomes] |
rs10180581 | 0.84[EUR][1000 genomes] |
rs10202023 | 0.91[EUR][1000 genomes] |
rs11675192 | 0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11675629 | 0.89[EUR][1000 genomes] |
rs11676655 | 0.87[EUR][1000 genomes] |
rs11678064 | 0.89[EUR][1000 genomes] |
rs11681517 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11681870 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11683123 | 0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11686018 | 0.96[EUR][1000 genomes] |
rs11686062 | 0.94[EUR][1000 genomes] |
rs11686861 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11690475 | 0.94[EUR][1000 genomes] |
rs11691490 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11691615 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs11691944 | 0.97[EUR][1000 genomes] |
rs11693233 | 0.80[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs11695761 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12693416 | 0.82[EUR][1000 genomes] |
rs12988744 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs12991386 | 0.96[EUR][1000 genomes] |
rs12991410 | 0.94[EUR][1000 genomes] |
rs12991698 | 0.85[EUR][1000 genomes] |
rs12998684 | 0.85[EUR][1000 genomes] |
rs13002265 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs13007661 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs13011116 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs13012137 | 0.94[EUR][1000 genomes] |
rs13014616 | 0.87[EUR][1000 genomes] |
rs13015041 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs13030170 | 0.84[EUR][1000 genomes] |
rs13030807 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13032463 | 0.94[EUR][1000 genomes] |
rs13033801 | 0.84[EUR][1000 genomes] |
rs13393583 | 0.91[EUR][1000 genomes] |
rs13429390 | 0.84[EUR][1000 genomes] |
rs13432887 | 0.85[EUR][1000 genomes] |
rs17206943 | 0.96[EUR][1000 genomes] |
rs17230036 | 0.85[EUR][1000 genomes] |
rs17230101 | 0.85[EUR][1000 genomes] |
rs2287607 | 0.84[EUR][1000 genomes] |
rs34000575 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs34087779 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs34093449 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34113655 | 0.99[EUR][1000 genomes] |
rs34152682 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs34191961 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34221764 | 0.99[EUR][1000 genomes] |
rs34338290 | 0.94[EUR][1000 genomes] |
rs34420134 | 0.89[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs34449658 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34537855 | 0.89[EUR][1000 genomes] |
rs34571837 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs34626145 | 0.94[EUR][1000 genomes] |
rs34631835 | 0.85[EUR][1000 genomes] |
rs34654071 | 0.94[EUR][1000 genomes] |
rs34661485 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs34826735 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs34877204 | 0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34879834 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs34969380 | 0.88[EUR][1000 genomes] |
rs35047001 | 0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs35061410 | 0.96[ASN][1000 genomes] |
rs35062319 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35066265 | 0.89[EUR][1000 genomes] |
rs35110878 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35165452 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35201815 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs35207414 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs35267530 | 0.94[EUR][1000 genomes] |
rs35289321 | 0.99[EUR][1000 genomes] |
rs35320505 | 0.94[EUR][1000 genomes] |
rs35537030 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs35638932 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35639419 | 0.94[EUR][1000 genomes] |
rs35781787 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35815004 | 0.87[EUR][1000 genomes] |
rs35847686 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35871462 | 0.80[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs35920523 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs36012390 | 0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs36065595 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs3752671 | 0.84[EUR][1000 genomes] |
rs61459829 | 0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs66508949 | 0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs67035495 | 1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs6708098 | 0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs6731674 | 0.87[EUR][1000 genomes] |
rs6739732 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs67432566 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs67629903 | 0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs67638453 | 0.87[EUR][1000 genomes] |
rs67784166 | 0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs67992386 | 0.87[EUR][1000 genomes] |
rs71430186 | 0.80[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs71432404 | 0.94[EUR][1000 genomes] |
rs71432408 | 0.93[EUR][1000 genomes] |
rs72896456 | 1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs7556993 | 0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7565527 | 0.84[EUR][1000 genomes] |
rs7584519 | 0.91[EUR][1000 genomes] |
rs7599251 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9789468 | 0.93[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv459982 | chr2:186213755-186475590 | Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv584012 | chr2:186213755-186475590 | ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv875527 | chr2:186272059-186475590 | Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv875528 | chr2:186301351-186475590 | Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
5 | nsv1004048 | chr2:186303297-186541503 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
6 | nsv875530 | chr2:186303530-186475590 | ZNF genes & repeats Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
7 | nsv875531 | chr2:186303530-186489537 | Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
8 | nsv875535 | chr2:186309738-186458903 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
9 | nsv875534 | chr2:186309738-186475590 | Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Enhancers Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
10 | nsv875536 | chr2:186309738-186504175 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
11 | nsv875539 | chr2:186345148-186475590 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
12 | nsv875540 | chr2:186345148-186583961 | Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
13 | nsv875541 | chr2:186345148-186598526 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
14 | nsv1006219 | chr2:186352780-186524793 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
15 | nsv584017 | chr2:186352959-186515328 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
16 | nsv584018 | chr2:186352959-186598526 | Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
17 | nsv916442 | chr2:186356363-186534152 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
18 | nsv875543 | chr2:186365918-186489537 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
19 | nsv1000814 | chr2:186391490-186520872 | Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
20 | nsv875544 | chr2:186396639-186458903 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:186433000-186447400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr2:186436000-186452200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
3 | chr2:186437000-186443800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |