Variant report
Variant | rs2497337 |
---|---|
Chromosome Location | chr10:94540286-94540287 |
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 |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000152804 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs10509646 | 1.00[CHB][hapmap];0.87[CHD][hapmap];0.81[JPT][hapmap];0.90[ASN][1000 genomes] |
rs2488065 | 0.85[ASN][1000 genomes] |
rs2497349 | 1.00[CHB][hapmap] |
rs7100186 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs7924271 | 0.82[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv3446249 | chr10:94374508-94549394 | Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 17 gene(s) | inside rSNPs | diseases |
2 | esv2761615 | chr10:94538960-94545531 | Enhancers Weak transcription Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |