Variant report
Variant | rs1246587 |
---|---|
Chromosome Location | chr4:75102648-75102649 |
allele | C/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 |
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(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10009707 | 0.85[EUR][1000 genomes] |
rs10013212 | 0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10017409 | 0.82[EUR][1000 genomes] |
rs10017417 | 0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs10018373 | 0.92[EUR][1000 genomes] |
rs10019396 | 0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs10023519 | 0.84[EUR][1000 genomes] |
rs10026687 | 0.84[EUR][1000 genomes] |
rs10028285 | 0.81[EUR][1000 genomes] |
rs10433673 | 0.92[EUR][1000 genomes] |
rs10938112 | 0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11724468 | 0.88[EUR][1000 genomes] |
rs11731340 | 0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs11737662 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs11945418 | 0.89[EUR][1000 genomes] |
rs1246575 | 0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1246577 | 0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1246578 | 0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs1246579 | 0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1246580 | 0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1246582 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1246584 | 0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1246586 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1246588 | 0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1246590 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1246591 | 0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes] |
rs1246594 | 0.91[EUR][1000 genomes] |
rs1246597 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs12500697 | 0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs1265327 | 0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs13116896 | 0.92[EUR][1000 genomes] |
rs13142241 | 0.90[EUR][1000 genomes] |
rs1371796 | 0.88[EUR][1000 genomes] |
rs1371797 | 0.84[EUR][1000 genomes] |
rs1380561 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs1460016 | 0.93[EUR][1000 genomes] |
rs1460017 | 0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs16850862 | 0.82[EUR][1000 genomes] |
rs17232394 | 0.84[EUR][1000 genomes] |
rs1964526 | 0.92[EUR][1000 genomes] |
rs2045618 | 0.88[EUR][1000 genomes] |
rs2061508 | 0.84[EUR][1000 genomes] |
rs2367555 | 0.90[EUR][1000 genomes] |
rs2367745 | 0.89[EUR][1000 genomes] |
rs28378517 | 0.87[EUR][1000 genomes] |
rs28436705 | 0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs28539097 | 0.84[EUR][1000 genomes] |
rs28592249 | 0.87[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs28644493 | 0.85[EUR][1000 genomes] |
rs28695994 | 0.93[EUR][1000 genomes] |
rs4371587 | 0.85[EUR][1000 genomes] |
rs4502653 | 0.84[EUR][1000 genomes] |
rs4577545 | 0.82[EUR][1000 genomes] |
rs4694184 | 0.87[EUR][1000 genomes] |
rs488440 | 0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs536541 | 0.84[EUR][1000 genomes] |
rs565831 | 0.84[EUR][1000 genomes] |
rs62312513 | 0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes] |
rs62312515 | 0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs62312545 | 0.84[EUR][1000 genomes] |
rs6446983 | 0.84[EUR][1000 genomes] |
rs6446984 | 0.84[EUR][1000 genomes] |
rs6446985 | 0.84[EUR][1000 genomes] |
rs6811214 | 0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs6819605 | 0.82[EUR][1000 genomes] |
rs6821664 | 0.85[EUR][1000 genomes] |
rs6854203 | 0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs6854723 | 0.84[EUR][1000 genomes] |
rs6858809 | 0.87[EUR][1000 genomes];0.88[ASN][1000 genomes] |
rs7659389 | 0.85[EUR][1000 genomes] |
rs7665105 | 0.85[EUR][1000 genomes] |
rs7670535 | 0.85[EUR][1000 genomes] |
rs7672588 | 0.84[EUR][1000 genomes] |
rs7676371 | 0.84[EUR][1000 genomes] |
rs7678292 | 0.85[EUR][1000 genomes] |
rs7681137 | 0.84[EUR][1000 genomes] |
rs7681763 | 0.84[EUR][1000 genomes] |
rs7681912 | 0.90[EUR][1000 genomes] |
rs7683181 | 0.90[EUR][1000 genomes] |
rs9992393 | 0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs9997322 | 0.84[EUR][1000 genomes] |
rs9997788 | 0.86[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv525980 | chr4:74731526-75382209 | Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 40 gene(s) | inside rSNPs | diseases |
2 | nsv1004768 | chr4:74774372-75109579 | Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
3 | nsv1006218 | chr4:74782324-75105424 | Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 25 gene(s) | inside rSNPs | diseases |
4 | nsv594683 | chr4:75013441-75106485 | Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
5 | nsv1013260 | chr4:75013441-75121643 | Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
6 | nsv1002907 | chr4:75013441-75131443 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
7 | nsv1004706 | chr4:75014770-75121643 | Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
8 | nsv594684 | chr4:75015750-75106485 | Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 14 gene(s) | inside rSNPs | diseases |
9 | nsv1009099 | chr4:75089233-75726206 | Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 34 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:75080600-75109600 | Weak transcription | Primary hematopoietic stem cells | blood |
2 | chr4:75086200-75117600 | Weak transcription | Duodenum Smooth Muscle | Duodenum |
3 | chr4:75091800-75103200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
4 | chr4:75093000-75105000 | Weak transcription | Lung | lung |
5 | chr4:75093000-75117400 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
6 | chr4:75097400-75117400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
7 | chr4:75097600-75103200 | Weak transcription | NHEK | skin |
8 | chr4:75099200-75103200 | Weak transcription | Hela-S3 | cervix |
9 | chr4:75101400-75105200 | Weak transcription | Primary hematopoietic stem cells G-CSF-mobilized Male | -- |
10 | chr4:75101400-75117600 | Weak transcription | Primary hematopoietic stem cells short term culture | blood |