Variant report
Variant | rs12530153 |
---|---|
Chromosome Location | chr6:119422682-119422683 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:3)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:3 , 50 per page) page:
1
No data |
No data |
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Variant related genes | Relation type |
---|---|
ENSG00000111879 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs12665481 | 0.88[AMR][1000 genomes] |
rs1360782 | 0.81[ASN][1000 genomes] |
rs4946393 | 0.88[AMR][1000 genomes] |
rs57363942 | 0.83[AMR][1000 genomes];0.94[ASN][1000 genomes] |
rs644640 | 0.84[CHB][hapmap] |
rs945197 | 0.83[AMR][1000 genomes] |
rs9481884 | 0.85[AMR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1030400 | chr6:119320153-119433830 | Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers | TF binding regionCpG islandChromatin interactive regionmiRNA | 30 gene(s) | inside rSNPs | diseases |
2 | nsv1025995 | chr6:119407742-119709548 | Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 21 gene(s) | inside rSNPs | diseases |
No data |