Variant report
Variant | rs7064626 |
---|---|
Chromosome Location | chrX:64234556-64234557 |
allele | A/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] |
---|---|
rs10126240 | 1.00[YRI][hapmap] |
rs11093854 | 0.96[YRI][hapmap] |
rs12389797 | 0.91[YRI][hapmap] |
rs1932206 | 0.95[YRI][hapmap] |
rs5964404 | 0.91[YRI][hapmap] |
rs5964406 | 0.95[YRI][hapmap] |
rs5964889 | 0.91[YRI][hapmap] |
rs5964890 | 0.96[YRI][hapmap] |
rs5964926 | 0.96[YRI][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv817451 | chrX:64049597-64916072 | Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
2 | nsv916714 | chrX:64178342-64589821 | Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNA | 10 gene(s) | inside rSNPs | diseases |
No data |