Variant report
Variant | rs7682889 |
---|---|
Chromosome Location | chr4:111187919-111187920 |
allele | A/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:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000170522 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs12499996 | 0.82[EUR][1000 genomes] |
rs12508536 | 0.85[EUR][1000 genomes] |
rs17041496 | 0.85[EUR][1000 genomes] |
rs2170552 | 0.91[AMR][1000 genomes];0.87[EUR][1000 genomes] |
rs34304604 | 0.83[EUR][1000 genomes] |
rs34605697 | 0.85[EUR][1000 genomes] |
rs4541589 | 0.85[EUR][1000 genomes] |
rs4557340 | 0.84[AMR][1000 genomes];0.91[EUR][1000 genomes] |
rs4585374 | 0.85[EUR][1000 genomes] |
rs4698764 | 0.84[AMR][1000 genomes];0.86[EUR][1000 genomes] |
rs4698817 | 0.86[EUR][1000 genomes] |
rs6533501 | 0.85[EUR][1000 genomes] |
rs6533503 | 0.85[EUR][1000 genomes] |
rs6533505 | 0.83[EUR][1000 genomes] |
rs7697518 | 0.84[AMR][1000 genomes];0.86[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 |