Variant report
Variant | rs4730569 |
---|---|
Chromosome Location | chr7:78547842-78547843 |
allele | A/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] |
---|---|
rs12705836 | 0.84[ASW][hapmap];0.87[TSI][hapmap] |
rs12705859 | 0.82[CHB][hapmap];0.86[JPT][hapmap] |
rs1624161 | 0.91[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes] |
rs1642888 | 0.83[CHD][hapmap];0.87[JPT][hapmap] |
rs17151725 | 0.84[ASW][hapmap];0.84[TSI][hapmap] |
rs17505 | 0.91[CHB][hapmap];0.85[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes] |
rs2052403 | 0.91[CHB][hapmap];0.95[JPT][hapmap] |
rs7797351 | 0.86[CHB][hapmap];0.86[CHD][hapmap];0.87[JPT][hapmap];0.82[ASN][1000 genomes] |
rs7799287 | 0.82[CHB][hapmap];0.86[CHD][hapmap];0.87[JPT][hapmap] |
rs987435 | 0.81[GIH][hapmap];0.87[JPT][hapmap] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv464598 | chr7:78492642-79483480 | Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |
2 | nsv607659 | chr7:78492642-79483480 | Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 15 gene(s) | inside rSNPs | diseases |