Variant report
Variant | rs73099493 |
---|---|
Chromosome Location | chr4:10340253-10340254 |
allele | A/C |
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 | chr4:10326481..10328401-chr4:10338341..10340263,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1558490 | 1.00[EUR][1000 genomes] |
rs2110026 | 1.00[EUR][1000 genomes] |
rs4379064 | 1.00[EUR][1000 genomes] |
rs55694260 | 1.00[EUR][1000 genomes] |
rs55767872 | 0.82[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs55784530 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs55820869 | 1.00[EUR][1000 genomes] |
rs55838007 | 0.82[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs55893553 | 1.00[EUR][1000 genomes] |
rs55917892 | 1.00[EUR][1000 genomes] |
rs55927832 | 1.00[EUR][1000 genomes] |
rs55972867 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs56016649 | 1.00[EUR][1000 genomes] |
rs56063732 | 1.00[EUR][1000 genomes] |
rs56070761 | 1.00[EUR][1000 genomes] |
rs56075212 | 0.82[AFR][1000 genomes] |
rs56077136 | 1.00[EUR][1000 genomes] |
rs56080915 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs56098146 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs56163461 | 1.00[EUR][1000 genomes] |
rs56215029 | 0.83[AFR][1000 genomes] |
rs56219221 | 1.00[EUR][1000 genomes] |
rs56221619 | 1.00[EUR][1000 genomes] |
rs56234106 | 1.00[EUR][1000 genomes] |
rs56253858 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs56358454 | 1.00[EUR][1000 genomes] |
rs56363374 | 1.00[EUR][1000 genomes] |
rs56786421 | 1.00[EUR][1000 genomes] |
rs56860554 | 1.00[EUR][1000 genomes] |
rs57120912 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs57483377 | 1.00[EUR][1000 genomes] |
rs57525975 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs57806546 | 1.00[EUR][1000 genomes] |
rs57868612 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs57944465 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs58129559 | 1.00[EUR][1000 genomes] |
rs58161541 | 1.00[EUR][1000 genomes] |
rs58500315 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs58517937 | 0.89[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs58535613 | 1.00[EUR][1000 genomes] |
rs58565838 | 1.00[EUR][1000 genomes] |
rs58690731 | 1.00[EUR][1000 genomes] |
rs58713079 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs58821154 | 0.83[AFR][1000 genomes] |
rs58881185 | 1.00[EUR][1000 genomes] |
rs58954581 | 0.83[AFR][1000 genomes] |
rs58980419 | 1.00[EUR][1000 genomes] |
rs59080844 | 1.00[EUR][1000 genomes] |
rs59119146 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs59439340 | 1.00[EUR][1000 genomes] |
rs59451589 | 1.00[EUR][1000 genomes] |
rs59611708 | 1.00[EUR][1000 genomes] |
rs59868112 | 1.00[EUR][1000 genomes] |
rs59972089 | 1.00[EUR][1000 genomes] |
rs60280725 | 0.85[AFR][1000 genomes] |
rs60340555 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs60367612 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs60408597 | 1.00[EUR][1000 genomes] |
rs60483101 | 1.00[EUR][1000 genomes] |
rs60513268 | 1.00[EUR][1000 genomes] |
rs60610004 | 1.00[EUR][1000 genomes] |
rs60711771 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs60739271 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs60807996 | 0.83[AFR][1000 genomes] |
rs60894502 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs61003749 | 1.00[EUR][1000 genomes] |
rs61076578 | 1.00[EUR][1000 genomes] |
rs61230832 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs61290503 | 1.00[EUR][1000 genomes] |
rs61308832 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs61412488 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs61516532 | 0.81[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs6447915 | 1.00[EUR][1000 genomes] |
rs6447916 | 1.00[EUR][1000 genomes] |
rs6447918 | 1.00[EUR][1000 genomes] |
rs6447924 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs6447925 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs6449444 | 1.00[EUR][1000 genomes] |
rs6814732 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs6820049 | 1.00[EUR][1000 genomes] |
rs6822248 | 1.00[EUR][1000 genomes] |
rs6825857 | 1.00[EUR][1000 genomes] |
rs6834163 | 1.00[EUR][1000 genomes] |
rs6835730 | 0.85[AFR][1000 genomes] |
rs6840182 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs6843292 | 1.00[EUR][1000 genomes] |
rs6845949 | 1.00[EUR][1000 genomes] |
rs6850854 | 0.83[AFR][1000 genomes] |
rs6855062 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73093996 | 1.00[EUR][1000 genomes] |
rs73093997 | 1.00[EUR][1000 genomes] |
rs73093998 | 1.00[EUR][1000 genomes] |
rs73096031 | 1.00[EUR][1000 genomes] |
rs73096037 | 1.00[EUR][1000 genomes] |
rs73096043 | 1.00[EUR][1000 genomes] |
rs73097526 | 1.00[EUR][1000 genomes] |
rs73097533 | 1.00[EUR][1000 genomes] |
rs73097543 | 1.00[EUR][1000 genomes] |
rs73097559 | 1.00[EUR][1000 genomes] |
rs73097575 | 1.00[EUR][1000 genomes] |
rs73097599 | 1.00[EUR][1000 genomes] |
rs73099415 | 1.00[EUR][1000 genomes] |
rs73099437 | 1.00[EUR][1000 genomes] |
rs73099447 | 1.00[EUR][1000 genomes] |
rs73099450 | 1.00[EUR][1000 genomes] |
rs73099482 | 1.00[EUR][1000 genomes] |
rs73099490 | 0.86[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73099491 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73099494 | 0.86[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73099495 | 0.86[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73101218 | 1.00[EUR][1000 genomes] |
rs73101226 | 0.82[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73101228 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73101230 | 1.00[EUR][1000 genomes] |
rs73101232 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73101234 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73101239 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73101240 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73101242 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73101243 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73101270 | 1.00[EUR][1000 genomes] |
rs73101271 | 1.00[EUR][1000 genomes] |
rs73101281 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73103039 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73103042 | 1.00[EUR][1000 genomes] |
rs73103046 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73103048 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73103065 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73103070 | 0.83[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73103083 | 1.00[EUR][1000 genomes] |
rs73103095 | 0.83[AFR][1000 genomes] |
rs73103097 | 0.81[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73104904 | 0.85[AFR][1000 genomes] |
rs73104907 | 0.85[AFR][1000 genomes] |
rs73104910 | 0.83[AFR][1000 genomes] |
rs73104913 | 0.83[AFR][1000 genomes] |
rs73104926 | 1.00[EUR][1000 genomes] |
rs73104942 | 1.00[EUR][1000 genomes] |
rs73104947 | 1.00[EUR][1000 genomes] |
rs73107014 | 1.00[EUR][1000 genomes] |
rs73809246 | 1.00[EUR][1000 genomes] |
rs73809251 | 1.00[EUR][1000 genomes] |
rs73809255 | 1.00[EUR][1000 genomes] |
rs73809296 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7664646 | 1.00[EUR][1000 genomes] |
rs7666449 | 1.00[EUR][1000 genomes] |
rs7669855 | 1.00[EUR][1000 genomes] |
rs7675919 | 1.00[EUR][1000 genomes] |
rs7678213 | 1.00[EUR][1000 genomes] |
rs7681751 | 1.00[EUR][1000 genomes] |
rs7682993 | 1.00[EUR][1000 genomes] |
rs7683842 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7684600 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7689258 | 1.00[EUR][1000 genomes] |
rs7692594 | 0.85[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7694351 | 1.00[EUR][1000 genomes] |
rs7698269 | 1.00[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 | nsv593695 | chr4:10138470-10345548 | Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 16 gene(s) | inside rSNPs | diseases |
20 | 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 |
21 | 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 |
22 | 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 |
23 | 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 |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:10337400-10343000 | Weak transcription | K562 | blood |
2 | chr4:10338800-10346800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
3 | chr4:10339200-10346800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
4 | chr4:10339400-10346800 | Weak transcription | NHEK | skin |
5 | chr4:10339800-10345400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
6 | chr4:10340000-10346400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |