Variant report
Variant | rs73221404 |
---|---|
Chromosome Location | chr7:124242447-124242448 |
allele | C/T |
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:
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No data |
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Variant related genes | Relation type |
---|---|
ENSG00000207214 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs1917357 | 1.00[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs61617280 | 1.00[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs73219089 | 0.93[EUR][1000 genomes] |
rs73219092 | 0.93[EUR][1000 genomes] |
rs73221403 | 0.98[AFR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes] |
rs73221429 | 0.85[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv429809 | chr7:123937674-124835925 | Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 49 gene(s) | inside rSNPs | diseases |
2 | nsv831118 | chr7:124172267-124347527 | Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv1031885 | chr7:124236838-124268655 | Enhancers Weak transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |