Variant report
Variant | rs10761282 |
---|---|
Chromosome Location | chr9:96586175-96586176 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
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Variant related genes | Relation type |
---|---|
ENSG00000263875 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10122041 | 0.92[CEU][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs10123836 | 0.96[CEU][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs10821229 | 0.89[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs13288708 | 0.80[EUR][1000 genomes] |
rs2398874 | 0.80[EUR][1000 genomes] |
rs3957506 | 0.93[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs3996254 | 0.93[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs4354374 | 0.81[EUR][1000 genomes] |
rs4744287 | 0.91[CEU][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs57882762 | 0.90[AMR][1000 genomes];0.99[EUR][1000 genomes] |
rs7869328 | 0.92[AMR][1000 genomes];0.96[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv1824724 | chr9:96582360-96598551 | Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Enhancers ZNF genes & repeats | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |