Variant report
Variant | rs13109847 |
---|---|
Chromosome Location | chr4:10346245-10346246 |
allele | C/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 | chr4:10181069..10182933-chr4:10345413..10347984,3 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10489069 | 0.80[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs10489079 | 0.87[CEU][hapmap] |
rs10489080 | 1.00[ASW][hapmap];0.87[CEU][hapmap];0.85[GIH][hapmap];0.83[MEX][hapmap];1.00[MKK][hapmap];0.88[TSI][hapmap] |
rs12500891 | 0.87[CEU][hapmap];0.83[MEX][hapmap];0.85[TSI][hapmap] |
rs12513165 | 0.87[CEU][hapmap];0.81[EUR][1000 genomes] |
rs13123672 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13142790 | 0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs13145430 | 0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[MKK][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17385872 | 1.00[ASW][hapmap];0.87[CEU][hapmap];0.83[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.88[TSI][hapmap] |
rs17409460 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs17410735 | 0.87[CEU][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs17418415 | 0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17419612 | 0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs17419975 | 0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17420513 | 0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17420562 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17474174 | 0.90[EUR][1000 genomes] |
rs17474238 | 0.90[EUR][1000 genomes] |
rs17475334 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs17477561 | 0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17478453 | 0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17479487 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1860903 | 1.00[ASW][hapmap];0.87[CEU][hapmap];0.85[GIH][hapmap];0.83[MEX][hapmap];1.00[MKK][hapmap];0.85[TSI][hapmap] |
rs2192094 | 0.87[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs35698830 | 0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35930609 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs36148106 | 1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4302456 | 0.86[EUR][1000 genomes] |
rs4302457 | 1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |
rs56105317 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs56106853 | 1.00[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs56126151 | 1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs56278885 | 0.82[EUR][1000 genomes] |
rs56335442 | 0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs56383050 | 0.84[EUR][1000 genomes] |
rs62286357 | 0.87[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs62286662 | 0.80[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs62286666 | 0.92[EUR][1000 genomes] |
rs62286698 | 0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62286699 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62286701 | 0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62286702 | 0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62286704 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62286706 | 1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62286707 | 0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62286709 | 0.88[AMR][1000 genomes];0.93[EUR][1000 genomes] |
rs62286710 | 0.89[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs62286733 | 0.92[AMR][1000 genomes];0.97[EUR][1000 genomes] |
rs62286737 | 0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs62286738 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs62286739 | 0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs62286740 | 0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs62286741 | 1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs62286744 | 0.82[EUR][1000 genomes] |
rs62286745 | 0.82[EUR][1000 genomes] |
rs62286746 | 0.82[AMR][1000 genomes];0.89[EUR][1000 genomes] |
rs62286748 | 1.00[AFR][1000 genomes];0.88[EUR][1000 genomes] |
rs62286749 | 1.00[AFR][1000 genomes];0.89[EUR][1000 genomes] |
rs62288062 | 0.87[AFR][1000 genomes];0.80[EUR][1000 genomes] |
rs62288123 | 0.80[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs62288124 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes] |
rs62288125 | 0.83[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs62288471 | 0.89[EUR][1000 genomes] |
rs62288477 | 1.00[AFR][1000 genomes];0.82[EUR][1000 genomes] |
rs62288478 | 1.00[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs62288479 | 1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs62288481 | 0.86[EUR][1000 genomes] |
rs6449453 | 0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6834574 | 0.87[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs6838644 | 0.86[CEU][hapmap];0.82[EUR][1000 genomes] |
rs6838846 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6853659 | 0.88[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs73222577 | 0.87[AFR][1000 genomes];0.85[EUR][1000 genomes] |
rs73224405 | 0.82[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs73224416 | 0.83[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs73224422 | 0.82[AMR][1000 genomes];0.92[EUR][1000 genomes] |
rs7659717 | 0.81[CEU][hapmap] |
rs7661555 | 0.80[EUR][1000 genomes] |
rs7666514 | 0.85[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs7675450 | 0.82[EUR][1000 genomes] |
rs7683755 | 0.87[CEU][hapmap];0.92[EUR][1000 genomes] |
rs887729 | 0.87[CEU][hapmap];0.85[GIH][hapmap];0.85[TSI][hapmap] |
rs887735 | 0.80[CEU][hapmap];0.84[GIH][hapmap];0.85[TSI][hapmap] |
rs929577 | 0.87[CEU][hapmap];0.83[MEX][hapmap];1.00[MKK][hapmap];0.91[TSI][hapmap];1.00[AFR][1000 genomes];0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv878681 | chr4:9802853-10397327 | Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 51 gene(s) | inside rSNPs | diseases |
2 | nsv997941 | chr4:9805223-10493388 | Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 54 gene(s) | inside rSNPs | diseases |
3 | nsv1008649 | chr4:9805223-10589802 | Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 56 gene(s) | inside rSNPs | diseases |
4 | nsv1000587 | chr4:9805223-10610752 | Flanking Active TSS Enhancers Genic enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 56 gene(s) | inside rSNPs | diseases |
5 | nsv537022 | chr4:9805223-10610752 | Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 56 gene(s) | inside rSNPs | diseases |
6 | nsv1003454 | chr4:9805223-10710990 | Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 58 gene(s) | inside rSNPs | diseases |
7 | nsv537023 | chr4:9805223-10710990 | Weak transcription Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 58 gene(s) | inside rSNPs | diseases |
8 | nsv1004801 | chr4:9814720-10674528 | Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 57 gene(s) | inside rSNPs | diseases |
9 | nsv537024 | chr4:9814720-10674528 | Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 57 gene(s) | inside rSNPs | diseases |
10 | nsv931483 | chr4:9814721-10716463 | Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 58 gene(s) | inside rSNPs | diseases |
11 | nsv1009972 | chr4:9903566-10710990 | Genic enhancers Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 58 gene(s) | inside rSNPs | diseases |
12 | nsv537027 | chr4:9903566-10710990 | Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 58 gene(s) | inside rSNPs | diseases |
13 | nsv1010620 | chr4:9937123-10686682 | Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 57 gene(s) | inside rSNPs | diseases |
14 | nsv530280 | chr4:9947818-10940041 | Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 66 gene(s) | inside rSNPs | diseases |
15 | nsv532706 | chr4:9948018-10451450 | Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 50 gene(s) | inside rSNPs | diseases |
16 | nsv878691 | chr4:9966477-10418078 | Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 50 gene(s) | inside rSNPs | diseases |
17 | nsv869057 | chr4:10013411-10875454 | Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 65 gene(s) | inside rSNPs | diseases |
18 | nsv997936 | chr4:10040713-11009045 | Weak transcription Flanking Active TSS Enhancers Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 65 gene(s) | inside rSNPs | diseases |
19 | nsv1000177 | chr4:10212245-10557776 | Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
20 | nsv537037 | chr4:10212245-10557776 | Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 18 gene(s) | inside rSNPs | diseases |
21 | nsv1007206 | chr4:10229982-10362490 | Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
22 | nsv829858 | chr4:10300236-10492716 | Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
23 | esv2757921 | chr4:10343699-10545800 | Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
24 | esv2759223 | chr4:10343699-10545800 | Strong transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 13 gene(s) | inside rSNPs | diseases |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:10338800-10346800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
2 | chr4:10339200-10346800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
3 | chr4:10339400-10346800 | Weak transcription | NHEK | skin |
4 | chr4:10340000-10346400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
5 | chr4:10345400-10348600 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
6 | chr4:10345800-10347000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
7 | chr4:10345800-10347200 | Enhancers | K562 | blood |
8 | chr4:10346000-10347000 | Weak transcription | HMEC | breast |
9 | chr4:10346200-10348200 | Enhancers | Placenta | Placenta |