Variant report
Variant | rs4697749 |
---|---|
Chromosome Location | chr4:10347284-10347285 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
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rs_ID | r2[population] |
---|---|
rs10010656 | 0.84[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10014800 | 0.93[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10023177 | 0.83[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs10029208 | 0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs10031806 | 0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1017124 | 0.84[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1035051 | 0.80[ASN][1000 genomes] |
rs1035052 | 0.80[ASN][1000 genomes] |
rs10489068 | 0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10938768 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs10939801 | 0.87[ASN][1000 genomes] |
rs10939818 | 0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs10939829 | 0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs11724760 | 0.85[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs11727366 | 0.84[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs11730940 | 0.87[ASN][1000 genomes] |
rs11732092 | 0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11735623 | 0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs11931317 | 0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11932349 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11937220 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs11943393 | 0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs11945358 | 0.86[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs12501750 | 0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs1544599 | 0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs16897170 | 0.81[ASN][1000 genomes] |
rs1860895 | 0.84[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs1860904 | 0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1860905 | 0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1860907 | 0.84[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1964268 | 0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1974647 | 0.92[ASN][1000 genomes] |
rs2003565 | 0.86[ASN][1000 genomes] |
rs2007103 | 0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs2024281 | 0.86[ASN][1000 genomes] |
rs2024282 | 0.86[ASN][1000 genomes] |
rs2080077 | 0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2098235 | 0.81[ASN][1000 genomes] |
rs2098236 | 0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2098237 | 0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs2110027 | 0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs2192084 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2192101 | 0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs28507715 | 0.87[ASN][1000 genomes] |
rs2868936 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs28705061 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs34103396 | 0.80[ASN][1000 genomes] |
rs4282174 | 0.83[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4306950 | 0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs4463062 | 0.86[ASN][1000 genomes] |
rs4522862 | 0.84[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4541507 | 0.85[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4610325 | 0.80[AMR][1000 genomes];0.82[ASN][1000 genomes] |
rs4697744 | 0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4697747 | 0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4697748 | 0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4697750 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4697751 | 0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4697752 | 1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4697984 | 0.83[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4697986 | 0.85[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs4698017 | 0.88[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4698018 | 0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4698025 | 0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4698028 | 0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs4698033 | 0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs4698037 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4698041 | 0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs4698043 | 0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs4698049 | 0.86[ASN][1000 genomes] |
rs56170676 | 0.87[ASN][1000 genomes] |
rs59420943 | 0.84[ASN][1000 genomes] |
rs6447945 | 0.83[ASN][1000 genomes] |
rs6449445 | 0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6449449 | 0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6449451 | 0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6449452 | 0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6449454 | 0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6810699 | 0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes] |
rs6813712 | 0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6819959 | 0.83[ASN][1000 genomes] |
rs6839820 | 0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6849037 | 0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6849583 | 0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6851536 | 0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6853056 | 0.84[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs6856707 | 0.85[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6857135 | 0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs727995 | 0.86[ASN][1000 genomes] |
rs7441343 | 0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs757628 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs759024 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs759027 | 0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs759031 | 0.87[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7661209 | 0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs7670709 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7675945 | 0.83[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs7677806 | 0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7680825 | 0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs7685241 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7688090 | 0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs769091 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes] |
rs7697246 | 0.86[ASN][1000 genomes] |
rs917827 | 0.84[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs984723 | 0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs9985952 | 0.86[ASN][1000 genomes] |
rs9990701 | 0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs9994176 | 0.86[ASN][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 | chr4:10345400-10348600 | Enhancers | Foreskin Keratinocyte Primary Cells skin02 | Skin |
2 | chr4:10346200-10348200 | Enhancers | Placenta | Placenta |
3 | chr4:10346400-10348800 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
4 | chr4:10346800-10347600 | Enhancers | Lung | lung |
5 | chr4:10346800-10348600 | Enhancers | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
6 | chr4:10346800-10348600 | Enhancers | Placenta Amnion | Placenta Amnion |
7 | chr4:10346800-10348600 | Enhancers | NHEK | skin |
8 | chr4:10347000-10348600 | Enhancers | Foreskin Keratinocyte Primary Cells skin03 | Skin |
9 | chr4:10347000-10349400 | Enhancers | HMEC | breast |
10 | chr4:10347200-10347800 | Flanking Active TSS | K562 | blood |
11 | chr4:10347200-10348400 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
12 | chr4:10347200-10348600 | Enhancers | hESC Derived CD56+ Mesoderm Cultured Cells | ES cell derived |