Variant report
| Variant | rs12188716 |
|---|---|
| Chromosome Location | chr5:92784778-92784779 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr5:92743600-92799200 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 2 | chr5:92760200-92798000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 3 | chr5:92767400-92797000 | Weak transcription | Fetal Brain Male | brain |
| 4 | chr5:92770000-92797800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 5 | chr5:92775200-92787400 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 6 | chr5:92777800-92792600 | Weak transcription | Fetal Lung | lung |
| 7 | chr5:92778000-92797400 | Weak transcription | Muscle Satellite Cultured Cells | -- |
| 8 | chr5:92778400-92793400 | Weak transcription | Fetal Stomach | stomach |
| 9 | chr5:92784000-92795000 | Weak transcription | HSMM | muscle |
| 10 | chr5:92784600-92795400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
