Variant report
Variant | rs11679158 |
---|---|
Chromosome Location | chr2:142519610-142519611 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:1 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr2:142519003..142520660-chr2:142522253..142524916,2 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1009398 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes] |
rs10183908 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs10193397 | 0.85[CEU][hapmap] |
rs10460250 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs10496896 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes] |
rs10496898 | 1.00[CHB][hapmap];0.85[JPT][hapmap] |
rs13416257 | 0.91[CHB][hapmap] |
rs1437345 | 0.95[CHB][hapmap];0.95[JPT][hapmap] |
rs1595318 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs16847120 | 0.91[CHB][hapmap];0.82[ASN][1000 genomes] |
rs1876595 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes] |
rs1898425 | 0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs1975286 | 0.91[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap] |
rs2009263 | 0.95[ASN][1000 genomes] |
rs2196597 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs2381153 | 1.00[CHB][hapmap];0.86[JPT][hapmap] |
rs28529494 | 0.81[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs4996425 | 0.84[AMR][1000 genomes];0.83[EUR][1000 genomes] |
rs6711195 | 0.83[ASN][1000 genomes] |
rs6720157 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs752451 | 0.95[ASN][1000 genomes] |
rs7558916 | 0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs7591783 | 1.00[CHB][hapmap];0.85[JPT][hapmap] |
rs7594617 | 0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs7598314 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs974974 | 0.95[CHB][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv834394 | chr2:142430225-142593264 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
2 | nsv530398 | chr2:142474842-142843839 | Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
3 | nsv459663 | chr2:142509570-142568465 | Weak transcription Enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
4 | nsv583236 | chr2:142509570-142568465 | Weak transcription Enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | n/a |
5 | nsv1004379 | chr2:142514657-142547597 | Weak transcription Enhancers Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | n/a |
No data |