Variant report
Variant | rs73714633 |
---|---|
Chromosome Location | chr7:116973011-116973012 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
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Variant related genes | Relation type |
---|---|
ENSG00000135269 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11980583 | 1.00[EUR][1000 genomes] |
rs11981502 | 1.00[EUR][1000 genomes] |
rs11983151 | 1.00[EUR][1000 genomes] |
rs17139469 | 1.00[EUR][1000 genomes] |
rs2106627 | 1.00[EUR][1000 genomes] |
rs4430033 | 1.00[EUR][1000 genomes] |
rs60356864 | 0.87[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs60412272 | 1.00[EUR][1000 genomes] |
rs6967851 | 1.00[EUR][1000 genomes] |
rs73470843 | 1.00[EUR][1000 genomes] |
rs73714631 | 0.95[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs73714637 | 0.95[AFR][1000 genomes];1.00[EUR][1000 genomes] |
rs7804397 | 1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv608256 | chr7:116928371-117040117 | Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 11 gene(s) | inside rSNPs | diseases |
No data |