Variant report
Variant | rs35822896 |
---|---|
Chromosome Location | chr7:138129947-138129948 |
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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Variant related genes | Relation type |
---|---|
ENSG00000214815 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs11765485 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12707386 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17169595 | 1.00[ASN][1000 genomes] |
rs57258992 | 1.00[ASN][1000 genomes] |
rs57833573 | 1.00[ASN][1000 genomes] |
rs57924062 | 1.00[ASN][1000 genomes] |
rs58054997 | 1.00[ASN][1000 genomes] |
rs59103803 | 0.81[ASN][1000 genomes] |
rs6970822 | 1.00[ASN][1000 genomes] |
rs7459225 | 1.00[ASN][1000 genomes] |
rs7808971 | 1.00[ASN][1000 genomes] |
rs7808984 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | esv34048 | chr7:137724092-138213119 | Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 35 gene(s) | inside rSNPs | diseases |
2 | nsv831153 | chr7:138078179-138265648 | Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 25 gene(s) | inside rSNPs | diseases |
3 | nsv970583 | chr7:138125511-138137818 | Weak transcription Enhancers ZNF genes & repeats | Chromatin interactive region | 2 gene(s) | inside rSNPs | diseases |
No data |