Variant report
Variant | rs4471850 |
---|---|
Chromosome Location | chr2:181825338-181825339 |
allele | G/T |
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)
No data |
No data |
(count:3 , 50 per page) page:
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No data |
No data |
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Variant related genes | Relation type |
---|---|
ENSG00000170035 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10183291 | 0.81[CHB][hapmap];0.81[JPT][hapmap];0.85[ASN][1000 genomes] |
rs10207300 | 0.84[ASN][1000 genomes] |
rs10432490 | 0.81[CHB][hapmap];0.85[JPT][hapmap] |
rs10803945 | 0.81[CHB][hapmap];0.81[JPT][hapmap] |
rs10930949 | 0.80[CHB][hapmap];0.85[JPT][hapmap] |
rs10930951 | 0.81[CHB][hapmap];0.85[JPT][hapmap] |
rs11680095 | 0.86[CHB][hapmap];0.81[JPT][hapmap] |
rs12475075 | 0.81[CHB][hapmap];0.81[JPT][hapmap] |
rs12477135 | 0.81[CHB][hapmap];0.81[JPT][hapmap] |
rs12613470 | 0.81[JPT][hapmap] |
rs12614444 | 0.81[CHB][hapmap];0.85[JPT][hapmap] |
rs34865829 | 0.80[ASN][1000 genomes] |
rs4618005 | 0.83[AFR][1000 genomes];0.95[ASN][1000 genomes] |
rs4638755 | 0.81[CHB][hapmap];0.85[JPT][hapmap];0.86[ASN][1000 genomes] |
rs873256 | 0.81[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv875476 | chr2:181767757-181854997 | Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 7 gene(s) | inside rSNPs | n/a |
2 | esv3347644 | chr2:181825260-181825583 | Inactive region | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
No data |