Variant report
Variant | rs1897532 |
---|---|
Chromosome Location | chr5:147576861-147576862 |
allele | C/G |
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] |
---|---|
rs10041939 | 0.86[EUR][1000 genomes] |
rs10052031 | 0.80[EUR][1000 genomes] |
rs10055396 | 0.82[EUR][1000 genomes] |
rs10058776 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs10059441 | 0.84[EUR][1000 genomes] |
rs10063951 | 0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10065999 | 0.92[CEU][hapmap] |
rs10067334 | 0.96[CEU][hapmap];0.84[EUR][1000 genomes] |
rs10068988 | 0.92[CEU][hapmap] |
rs10074328 | 0.82[EUR][1000 genomes] |
rs10077607 | 0.82[EUR][1000 genomes] |
rs10079388 | 0.96[EUR][1000 genomes] |
rs10079716 | 1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs10477363 | 0.83[EUR][1000 genomes] |
rs10491344 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs11168037 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs11168038 | 0.97[EUR][1000 genomes] |
rs11168039 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs11168041 | 0.97[EUR][1000 genomes] |
rs11743040 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs11743518 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs11743523 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs11745313 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs11748034 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12188857 | 1.00[CEU][hapmap];0.98[EUR][1000 genomes] |
rs12189210 | 0.92[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs12332436 | 0.96[CEU][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12332677 | 0.96[CEU][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12515246 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12515885 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12516461 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12519059 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12519106 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12519629 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12521387 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs12522694 | 0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs12653723 | 0.81[EUR][1000 genomes] |
rs12653724 | 0.81[EUR][1000 genomes] |
rs12717963 | 0.87[EUR][1000 genomes] |
rs13154742 | 0.82[EUR][1000 genomes] |
rs13174534 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs13174816 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs13174845 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs13175245 | 0.98[EUR][1000 genomes] |
rs13179181 | 0.89[EUR][1000 genomes] |
rs13185600 | 0.97[EUR][1000 genomes] |
rs13360182 | 0.88[CEU][hapmap] |
rs1368305 | 0.97[EUR][1000 genomes] |
rs1368306 | 0.96[CEU][hapmap];0.97[EUR][1000 genomes] |
rs1432689 | 0.92[CEU][hapmap];0.97[EUR][1000 genomes] |
rs1558410 | 0.83[EUR][1000 genomes] |
rs17096690 | 1.00[CEU][hapmap];0.99[EUR][1000 genomes] |
rs17096693 | 0.99[EUR][1000 genomes] |
rs17107871 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs1812484 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes] |
rs1897533 | 0.97[EUR][1000 genomes] |
rs1974627 | 0.83[EUR][1000 genomes] |
rs1974628 | 0.83[EUR][1000 genomes] |
rs1974629 | 0.83[EUR][1000 genomes] |
rs2017896 | 0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2159661 | 0.83[EUR][1000 genomes] |
rs2191680 | 0.93[CEU][hapmap] |
rs2191681 | 0.83[EUR][1000 genomes] |
rs2400493 | 0.83[EUR][1000 genomes] |
rs2400494 | 0.83[EUR][1000 genomes] |
rs2400495 | 0.83[EUR][1000 genomes] |
rs2400496 | 0.83[EUR][1000 genomes] |
rs2400497 | 0.83[EUR][1000 genomes] |
rs2400498 | 0.83[EUR][1000 genomes] |
rs28406596 | 0.97[EUR][1000 genomes] |
rs28624399 | 0.97[EUR][1000 genomes] |
rs28667181 | 0.97[EUR][1000 genomes] |
rs28701955 | 0.82[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs34211205 | 0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs34258096 | 0.84[EUR][1000 genomes] |
rs34339574 | 0.83[EUR][1000 genomes] |
rs34506706 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs35217112 | 0.84[EUR][1000 genomes] |
rs35491588 | 0.85[EUR][1000 genomes] |
rs35507985 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs35696310 | 0.82[EUR][1000 genomes] |
rs36056267 | 0.84[EUR][1000 genomes] |
rs4133459 | 0.97[EUR][1000 genomes] |
rs4254894 | 0.92[CEU][hapmap] |
rs4259160 | 0.83[EUR][1000 genomes] |
rs4269285 | 0.92[CEU][hapmap] |
rs4270684 | 0.83[EUR][1000 genomes] |
rs4452547 | 0.83[EUR][1000 genomes] |
rs4498243 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs4499819 | 0.92[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs4705231 | 0.97[EUR][1000 genomes] |
rs4705232 | 0.97[EUR][1000 genomes] |
rs4705233 | 0.97[EUR][1000 genomes] |
rs4705234 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs6580532 | 0.82[EUR][1000 genomes] |
rs6580533 | 0.82[EUR][1000 genomes] |
rs6580534 | 0.80[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs6580535 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs6580536 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs6860003 | 0.82[EUR][1000 genomes] |
rs6864124 | 0.86[EUR][1000 genomes] |
rs6865006 | 0.97[EUR][1000 genomes] |
rs6865474 | 1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs6867695 | 0.85[EUR][1000 genomes] |
rs6868569 | 0.86[EUR][1000 genomes] |
rs6869054 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs6870548 | 0.84[EUR][1000 genomes] |
rs6871633 | 0.84[EUR][1000 genomes] |
rs6875563 | 0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6881658 | 0.92[CEU][hapmap] |
rs6884944 | 0.82[EUR][1000 genomes] |
rs6895745 | 0.92[CEU][hapmap] |
rs6896988 | 0.84[EUR][1000 genomes] |
rs7442844 | 0.97[EUR][1000 genomes] |
rs7442875 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs7444240 | 0.80[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs7445428 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs7445725 | 0.83[EUR][1000 genomes] |
rs7448271 | 0.97[EUR][1000 genomes] |
rs7449160 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs767568 | 0.83[EUR][1000 genomes] |
rs767569 | 0.83[EUR][1000 genomes] |
rs767570 | 0.83[EUR][1000 genomes] |
rs7702990 | 0.86[EUR][1000 genomes] |
rs7703690 | 0.84[EUR][1000 genomes] |
rs7703761 | 0.83[EUR][1000 genomes] |
rs7705007 | 0.80[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs7716861 | 0.86[EUR][1000 genomes] |
rs7717699 | 0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs7719535 | 0.84[EUR][1000 genomes] |
rs7732604 | 0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9325084 | 0.83[EUR][1000 genomes] |
rs9325087 | 0.86[EUR][1000 genomes] |
rs9325088 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs963016 | 0.80[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs9885020 | 0.82[EUR][1000 genomes] |
rs9885270 | 0.82[EUR][1000 genomes] |
rs9885451 | 0.96[CEU][hapmap];0.92[JPT][hapmap];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv883015 | chr5:147404281-147751035 | Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 17 gene(s) | inside rSNPs | diseases |
2 | nsv830515 | chr5:147460852-147602247 | Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv980947 | chr5:147571596-147583858 | Enhancers Flanking Active TSS Weak transcription Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
4 | esv1845496 | chr5:147576457-147586789 | Weak transcription Active TSS Enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr5:147572200-147582000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr5:147573200-147584000 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
3 | chr5:147576000-147581000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
4 | chr5:147576200-147581400 | Weak transcription | NHEK | skin |
5 | chr5:147576600-147582400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |