Variant report
Variant | rs1689511 |
---|---|
Chromosome Location | chr12:56467385-56467386 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr12:56437000-56472800 | Weak transcription | Right Atrium | heart |
2 | chr12:56454400-56467800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
3 | chr12:56466200-56472400 | Weak transcription | Placenta Amnion | Placenta Amnion |
4 | chr12:56466400-56467400 | Weak transcription | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
5 | chr12:56466400-56467400 | Weak transcription | NHEK | skin |
6 | chr12:56466400-56471800 | Weak transcription | Hela-S3 | cervix |
7 | chr12:56466400-56472600 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
8 | chr12:56466600-56472600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
9 | chr12:56466600-56472800 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
10 | chr12:56467000-56468000 | Weak transcription | HepG2 | liver |