Variant report
Variant | rs13105073 |
---|---|
Chromosome Location | chr4:111188725-111188726 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:2)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
(count:2 , 50 per page) page:
1
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000250594 | TF binding region |
ENSG00000170522 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs34839006 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs35499292 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs71603067 | 1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs71603069 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv869392 | chr4:110945459-111235071 | Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
No data |