Variant report
Variant | rs6854192 |
---|---|
Chromosome Location | chr4:172791492-172791493 |
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 |
No data |
(count:2 , 50 per page) page:
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rs_ID | r2[population] |
---|---|
rs10031122 | 0.84[CEU][hapmap] |
rs10866351 | 0.80[CEU][hapmap] |
rs11931247 | 0.82[CEU][hapmap] |
rs13106824 | 0.81[CEU][hapmap] |
rs13130415 | 0.93[CEU][hapmap];0.80[CHB][hapmap];0.87[JPT][hapmap] |
rs1485863 | 0.82[CEU][hapmap] |
rs1485867 | 1.00[CEU][hapmap];0.85[CHB][hapmap];0.93[JPT][hapmap] |
rs179641 | 0.82[CEU][hapmap] |
rs189146 | 0.82[CEU][hapmap] |
rs332982 | 0.81[CEU][hapmap] |
rs332983 | 0.82[CEU][hapmap] |
rs332992 | 0.82[CEU][hapmap] |
rs332995 | 0.82[CEU][hapmap] |
rs332996 | 0.82[CEU][hapmap] |
rs333002 | 0.86[CEU][hapmap] |
rs6818985 | 1.00[CEU][hapmap];0.85[CHB][hapmap];0.87[JPT][hapmap] |
rs6825635 | 1.00[CEU][hapmap];0.90[CHB][hapmap];0.87[JPT][hapmap] |
rs6832294 | 0.82[CEU][hapmap] |
rs6839553 | 0.87[CEU][hapmap] |
rs6845054 | 0.82[CEU][hapmap] |
rs7666494 | 0.87[CEU][hapmap];0.87[JPT][hapmap] |
rs7690646 | 0.82[CEU][hapmap] |
rs9998139 | 0.82[CEU][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1022527 | chr4:172547732-173236939 | Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
2 | nsv537357 | chr4:172547732-173236939 | Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
3 | nsv1024693 | chr4:172609237-173236939 | Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv527739 | chr4:172772005-172816200 | Weak transcription Enhancers Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv881602 | chr4:172772005-172867912 | Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |