Variant report
Variant | rs4912173 |
---|---|
Chromosome Location | chr1:58208267-58208268 |
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] |
---|---|
rs10493232 | 0.91[GIH][hapmap];0.85[TSI][hapmap];0.82[EUR][1000 genomes] |
rs11577095 | 0.86[MEX][hapmap];0.84[AMR][1000 genomes] |
rs1323822 | 0.91[GIH][hapmap];0.80[MEX][hapmap];0.85[TSI][hapmap];0.83[EUR][1000 genomes] |
rs1323823 | 0.91[GIH][hapmap];0.80[MEX][hapmap];0.85[TSI][hapmap];0.83[EUR][1000 genomes] |
rs1408139 | 0.91[GIH][hapmap];0.85[TSI][hapmap];0.82[EUR][1000 genomes] |
rs3118041 | 0.83[CHB][hapmap] |
rs3118043 | 0.83[CHB][hapmap] |
rs3118045 | 0.83[CHB][hapmap] |
rs3131729 | 0.89[CEU][hapmap];0.83[CHD][hapmap];0.86[JPT][hapmap];0.90[TSI][hapmap];0.85[EUR][1000 genomes] |
rs7534106 | 0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1015057 | chr1:57976993-58793962 | Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
2 | nsv530017 | chr1:58002290-58669736 | Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 9 gene(s) | inside rSNPs | diseases |
No data |