Variant report
| Variant | rs6990032 |
|---|---|
| Chromosome Location | chr8:103730582-103730583 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr8:103713200-103733600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr8:103723600-103733600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 3 | chr8:103728800-103733600 | Weak transcription | Esophagus | oesophagus |
| 4 | chr8:103729000-103731400 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
| 5 | chr8:103729000-103733200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 6 | chr8:103729200-103733600 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 7 | chr8:103729400-103732000 | Weak transcription | HMEC | breast |
| 8 | chr8:103729400-103740200 | Weak transcription | Stomach Mucosa | stomach |
| 9 | chr8:103730200-103733000 | Weak transcription | Placenta | Placenta |
| 10 | chr8:103730400-103736000 | Weak transcription | K562 | blood |
