Variant report
Variant | rs72616951 |
---|---|
Chromosome Location | chr4:128708209-128708210 |
allele | G/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10493145 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10493146 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10493148 | 0.82[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs11935472 | 0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1355927 | 0.86[EUR][1000 genomes] |
rs1380155 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1514313 | 0.86[EUR][1000 genomes] |
rs1514314 | 0.86[EUR][1000 genomes] |
rs1514315 | 0.86[EUR][1000 genomes] |
rs16997978 | 0.83[ASN][1000 genomes] |
rs17012525 | 0.86[EUR][1000 genomes] |
rs17012586 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs17012601 | 0.95[EUR][1000 genomes];0.95[ASN][1000 genomes] |
rs17012634 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17012654 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17012683 | 0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17012687 | 0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17012695 | 0.87[ASN][1000 genomes] |
rs17012703 | 0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs17012708 | 0.82[AMR][1000 genomes];0.87[ASN][1000 genomes] |
rs17012710 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs17012727 | 0.83[ASN][1000 genomes] |
rs17012743 | 0.81[ASN][1000 genomes] |
rs17012747 | 0.81[ASN][1000 genomes] |
rs17012750 | 0.81[ASN][1000 genomes] |
rs1841156 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1841157 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs1903106 | 0.95[EUR][1000 genomes] |
rs2007243 | 0.86[EUR][1000 genomes] |
rs2276980 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs2279071 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs2391185 | 0.95[EUR][1000 genomes] |
rs28570426 | 0.90[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs2893227 | 0.95[EUR][1000 genomes] |
rs35147318 | 0.95[EUR][1000 genomes] |
rs35858752 | 0.95[EUR][1000 genomes];0.81[ASN][1000 genomes] |
rs4422427 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs4456965 | 0.81[EUR][1000 genomes];0.87[ASN][1000 genomes] |
rs4508904 | 0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[ASN][1000 genomes] |
rs4513584 | 0.86[ASN][1000 genomes] |
rs4590052 | 0.95[EUR][1000 genomes];0.84[ASN][1000 genomes] |
rs4607232 | 0.81[ASN][1000 genomes] |
rs4618331 | 0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.81[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs56250604 | 0.83[ASN][1000 genomes] |
rs56763029 | 0.95[EUR][1000 genomes] |
rs56893530 | 0.82[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs57499646 | 0.82[AMR][1000 genomes];0.85[ASN][1000 genomes] |
rs57645489 | 0.81[ASN][1000 genomes] |
rs58486324 | 0.95[EUR][1000 genomes] |
rs60279389 | 0.81[ASN][1000 genomes] |
rs60404814 | 0.95[EUR][1000 genomes] |
rs60553863 | 0.95[EUR][1000 genomes] |
rs60666303 | 0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs60803593 | 0.95[EUR][1000 genomes] |
rs6850549 | 0.82[ASN][1000 genomes] |
rs6850726 | 0.81[ASN][1000 genomes] |
rs72616920 | 0.95[EUR][1000 genomes] |
rs72616921 | 0.95[EUR][1000 genomes] |
rs72616922 | 0.95[EUR][1000 genomes] |
rs72616923 | 0.95[EUR][1000 genomes] |
rs72616924 | 0.95[EUR][1000 genomes] |
rs72616925 | 0.95[EUR][1000 genomes] |
rs72616926 | 0.95[EUR][1000 genomes] |
rs72616927 | 0.95[EUR][1000 genomes] |
rs72616928 | 0.95[EUR][1000 genomes] |
rs72616929 | 0.95[EUR][1000 genomes] |
rs72616930 | 0.95[EUR][1000 genomes] |
rs72616931 | 0.95[EUR][1000 genomes] |
rs72616932 | 0.95[EUR][1000 genomes] |
rs72616933 | 0.95[EUR][1000 genomes] |
rs72616934 | 0.95[EUR][1000 genomes] |
rs72616935 | 0.95[EUR][1000 genomes] |
rs72616936 | 0.95[EUR][1000 genomes];0.82[ASN][1000 genomes] |
rs72616937 | 0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72616938 | 0.95[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs72616939 | 0.95[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs72616940 | 0.95[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs72616941 | 0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72616942 | 0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72616943 | 0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72616947 | 0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72616948 | 0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72616949 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72616950 | 0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs72616952 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs72616953 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72616954 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs72616955 | 0.83[ASN][1000 genomes] |
rs72616956 | 0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes] |
rs72616957 | 0.82[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs72616958 | 0.82[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs72616959 | 0.82[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs72616960 | 0.82[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs72616961 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
rs72616963 | 0.83[ASN][1000 genomes] |
rs72621863 | 0.86[EUR][1000 genomes] |
rs72621865 | 0.86[EUR][1000 genomes] |
rs72621866 | 0.86[EUR][1000 genomes] |
rs72621867 | 0.86[EUR][1000 genomes] |
rs72621868 | 0.86[EUR][1000 genomes] |
rs72621869 | 0.86[EUR][1000 genomes] |
rs72621871 | 0.86[EUR][1000 genomes] |
rs72621886 | 0.95[EUR][1000 genomes] |
rs72621891 | 0.95[EUR][1000 genomes] |
rs72621892 | 0.95[EUR][1000 genomes] |
rs72621893 | 0.95[EUR][1000 genomes] |
rs72621894 | 0.95[EUR][1000 genomes] |
rs72621895 | 0.95[EUR][1000 genomes] |
rs72621896 | 0.95[EUR][1000 genomes] |
rs72621897 | 0.95[EUR][1000 genomes] |
rs72621898 | 0.95[EUR][1000 genomes] |
rs72621899 | 0.95[EUR][1000 genomes] |
rs72621900 | 0.95[EUR][1000 genomes] |
rs72621901 | 0.95[EUR][1000 genomes] |
rs72621902 | 0.95[EUR][1000 genomes] |
rs72624503 | 0.95[EUR][1000 genomes] |
rs72624504 | 0.95[EUR][1000 genomes] |
rs72624505 | 0.95[EUR][1000 genomes] |
rs7439365 | 0.95[EUR][1000 genomes] |
rs7684815 | 0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv879915 | chr4:128167093-129150590 | Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 48 gene(s) | inside rSNPs | diseases |
2 | nsv817326 | chr4:128292216-128915201 | Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 29 gene(s) | inside rSNPs | diseases |
3 | nsv879917 | chr4:128478408-128841252 | Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
4 | nsv879921 | chr4:128554404-128766074 | Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
5 | nsv879922 | chr4:128554404-128901402 | Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 26 gene(s) | inside rSNPs | diseases |
6 | nsv879923 | chr4:128554404-129068179 | Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 44 gene(s) | inside rSNPs | diseases |
7 | esv1801492 | chr4:128566686-128934513 | Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
8 | esv1792644 | chr4:128566686-129133826 | Enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 44 gene(s) | inside rSNPs | diseases |
9 | esv1795770 | chr4:128566686-129145581 | Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 44 gene(s) | inside rSNPs | diseases |
10 | esv1793579 | chr4:128577439-128871309 | Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
11 | esv1792152 | chr4:128585215-128752829 | Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |
12 | nsv830057 | chr4:128591288-128788777 | Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 21 gene(s) | inside rSNPs | diseases |
13 | nsv879926 | chr4:128652227-128766074 | Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
14 | esv3431515 | chr4:128657260-128932577 | Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
15 | nsv879927 | chr4:128668850-128766074 | Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 19 gene(s) | inside rSNPs | diseases |
16 | nsv967683 | chr4:128707527-128710207 | Weak transcription Enhancers Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:128705000-128718200 | Weak transcription | Fetal Heart | heart |
2 | chr4:128705400-128731600 | Weak transcription | Pancreas | Pancrea |
3 | chr4:128705600-128713400 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
4 | chr4:128706000-128743600 | Weak transcription | Duodenum Smooth Muscle | Duodenum |
5 | chr4:128706200-128759800 | Weak transcription | Brain Cingulate Gyrus | brain |
6 | chr4:128706400-128716400 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
7 | chr4:128706400-128716600 | Weak transcription | Hela-S3 | cervix |
8 | chr4:128706400-128726200 | Weak transcription | HMEC | breast |
9 | chr4:128706400-128729800 | Weak transcription | NHEK | skin |
10 | chr4:128706400-128741600 | Weak transcription | K562 | blood |
11 | chr4:128707000-128726800 | Weak transcription | HepG2 | liver |
12 | chr4:128707200-128712800 | Weak transcription | Pancreatic Islets | Pancreatic Islet |
13 | chr4:128707200-128716600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
14 | chr4:128707800-128709800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
15 | chr4:128708000-128711000 | Weak transcription | Aorta | Aorta |
16 | chr4:128708000-128716400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |