Variant report
Variant | rs12101636 |
---|---|
Chromosome Location | chr15:83907499-83907500 |
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:
1
No data |
No data |
No data |
Variant related genes | Relation type |
---|---|
ENSG00000166503 | Chromatin interaction |
rs_ID | r2[population] |
---|---|
rs17158059 | 0.98[EUR][1000 genomes] |
rs17841157 | 0.98[EUR][1000 genomes] |
rs28360733 | 0.85[EUR][1000 genomes] |
rs28479708 | 0.98[EUR][1000 genomes] |
rs28523446 | 0.94[EUR][1000 genomes] |
rs28558700 | 0.94[EUR][1000 genomes] |
rs28567531 | 0.90[EUR][1000 genomes] |
rs7167364 | 0.91[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs7171743 | 0.94[EUR][1000 genomes] |
rs7173876 | 0.96[EUR][1000 genomes] |
rs72755995 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs72756000 | 0.87[AMR][1000 genomes] |
rs72758306 | 0.82[AMR][1000 genomes];0.94[EUR][1000 genomes] |
rs72758308 | 0.82[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs72758310 | 0.82[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs72758313 | 0.98[EUR][1000 genomes] |
rs72758323 | 0.98[EUR][1000 genomes] |
rs72758331 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes] |
rs72758346 | 0.87[AMR][1000 genomes] |
rs72758350 | 0.91[AMR][1000 genomes];0.98[EUR][1000 genomes] |
rs8026576 | 0.96[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv534418 | chr15:83770116-83960718 | Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 20 gene(s) | inside rSNPs | diseases |