Variant report
Variant | rs10867862 |
---|---|
Chromosome Location | chr9:85224136-85224137 |
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] |
---|---|
rs10122746 | 0.94[EUR][1000 genomes] |
rs10512132 | 0.94[ASN][1000 genomes] |
rs10512133 | 0.92[ASN][1000 genomes] |
rs11139640 | 0.82[EUR][1000 genomes] |
rs11139646 | 0.82[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11139650 | 0.85[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11139652 | 0.94[ASN][1000 genomes] |
rs11139653 | 0.85[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11139654 | 0.85[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs11139661 | 0.82[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs11139665 | 0.92[ASN][1000 genomes] |
rs11139682 | 0.81[ASN][1000 genomes] |
rs11139683 | 0.81[ASN][1000 genomes] |
rs17085704 | 0.82[EUR][1000 genomes] |
rs2001818 | 0.94[ASN][1000 genomes] |
rs73648460 | 0.85[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs73648462 | 0.82[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs73648463 | 0.85[EUR][1000 genomes];0.94[ASN][1000 genomes] |
rs73650741 | 0.82[EUR][1000 genomes] |
rs7853040 | 0.94[ASN][1000 genomes] |
rs7853471 | 0.94[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv831641 | chr9:85145561-85309589 | Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS | Chromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:85221200-85227000 | Weak transcription | Fetal Stomach | stomach |