Variant report
Variant | rs11004076 |
---|---|
Chromosome Location | chr10:55873902-55873903 |
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] |
---|---|
rs10490981 | 0.87[ASW][hapmap] |
rs10763068 | 0.81[CHD][hapmap];1.00[JPT][hapmap] |
rs10763075 | 0.87[ASW][hapmap];0.81[MKK][hapmap] |
rs10825234 | 0.81[CHD][hapmap] |
rs10825237 | 0.81[CHD][hapmap] |
rs10825242 | 0.88[CHD][hapmap];1.00[JPT][hapmap] |
rs10825243 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap] |
rs11004075 | 1.00[JPT][hapmap] |
rs12360522 | 0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs12413011 | 0.81[CHD][hapmap] |
rs12782364 | 1.00[JPT][hapmap] |
rs16905760 | 1.00[JPT][hapmap] |
rs4007262 | 1.00[ASN][1000 genomes] |
rs4007264 | 0.87[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.82[MEX][hapmap];0.91[MKK][hapmap];0.81[YRI][hapmap] |
rs4319419 | 1.00[CHB][hapmap];1.00[JPT][hapmap] |
rs4495798 | 0.87[ASW][hapmap] |
rs4625368 | 0.87[ASN][1000 genomes] |
rs4935500 | 1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.90[MKK][hapmap];0.91[TSI][hapmap];0.81[YRI][hapmap] |
rs73239954 | 0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs7904409 | 0.87[ASW][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];0.81[MKK][hapmap];0.81[YRI][hapmap];0.91[ASN][1000 genomes] |
rs7920089 | 0.87[ASW][hapmap];0.81[MKK][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv949692 | chr10:55502542-55893206 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv8667 | chr10:55803106-56022647 | Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
3 | nsv428557 | chr10:55815334-55988225 | Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
4 | nsv870252 | chr10:55823123-56029435 | Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv948730 | chr10:55845301-56093271 | ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
6 | nsv1035173 | chr10:55847066-56005288 | Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |