Variant report
Variant | rs10485436 |
---|---|
Chromosome Location | chr6:69615168-69615169 |
allele | C/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1008234 | 0.88[JPT][hapmap] |
rs1018436 | 0.88[JPT][hapmap] |
rs10223798 | 0.88[JPT][hapmap] |
rs10485434 | 0.88[JPT][hapmap] |
rs10485437 | 0.88[JPT][hapmap] |
rs11751644 | 0.84[JPT][hapmap] |
rs13191240 | 1.00[YRI][hapmap] |
rs13201188 | 0.88[JPT][hapmap] |
rs13204176 | 0.84[JPT][hapmap] |
rs13204246 | 0.86[JPT][hapmap] |
rs13207774 | 1.00[ASW][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.87[YRI][hapmap];0.82[ASN][1000 genomes] |
rs13210533 | 0.88[JPT][hapmap] |
rs13215030 | 0.88[JPT][hapmap] |
rs13217051 | 0.88[JPT][hapmap] |
rs17200696 | 0.88[JPT][hapmap] |
rs1889879 | 0.95[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes] |
rs1916767 | 0.86[JPT][hapmap] |
rs1916768 | 0.88[JPT][hapmap] |
rs1932615 | 0.88[JPT][hapmap] |
rs1932618 | 0.95[CHD][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap] |
rs2184723 | 0.88[JPT][hapmap] |
rs3823061 | 0.86[MEX][hapmap];1.00[YRI][hapmap] |
rs6455307 | 0.88[JPT][hapmap] |
rs6908180 | 0.86[MEX][hapmap] |
rs6919909 | 0.82[MEX][hapmap];0.87[TSI][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes] |
rs7755226 | 0.88[JPT][hapmap] |
rs7760666 | 0.88[JPT][hapmap] |
rs7761270 | 0.82[MEX][hapmap] |
rs9294813 | 0.88[JPT][hapmap] |
rs9360367 | 0.86[JPT][hapmap];0.88[AMR][1000 genomes];0.84[ASN][1000 genomes] |
rs9454643 | 0.88[JPT][hapmap] |
rs9454645 | 0.88[JPT][hapmap] |
rs996768 | 0.88[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv470831 | chr6:69581991-69654650 | Weak transcription Enhancers ZNF genes & repeats Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
2 | nsv886136 | chr6:69598297-69654650 | Weak transcription Strong transcription ZNF genes & repeats Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:69602800-69621000 | Weak transcription | Fetal Lung | lung |