Variant report
Variant | rs7065069 |
---|---|
Chromosome Location | chrX:64688876-64688877 |
allele | C/G |
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] |
---|---|
rs12395545 | 1.00[CHD][hapmap];1.00[GIH][hapmap] |
rs12395619 | 0.93[ASW][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.97[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap] |
rs12397033 | 1.00[TSI][hapmap] |
rs2038284 | 1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap] |
rs2038285 | 1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap] |
rs5964442 | 1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap] |
rs5964443 | 1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap] |
rs5964961 | 0.95[YRI][hapmap] |
rs5964981 | 0.92[ASW][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.88[MKK][hapmap];0.86[YRI][hapmap] |
rs5964989 | 1.00[GIH][hapmap] |
rs5964990 | 1.00[GIH][hapmap] |
rs6524979 | 1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap] |
rs7050592 | 1.00[TSI][hapmap] |
rs7884225 | 0.92[ASW][hapmap];0.94[MKK][hapmap];0.86[YRI][hapmap] |
rs959215 | 1.00[GIH][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 | esv3432596 | chrX:64670980-64705458 | Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS | TF binding regionChromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |