Variant report
| Variant | rs56830331 |
|---|---|
| Chromosome Location | chr6:37368436-37368437 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:37350000-37368600 | Weak transcription | Fetal Heart | heart |
| 2 | chr6:37359000-37372600 | Weak transcription | Stomach Mucosa | stomach |
| 3 | chr6:37359600-37374000 | Weak transcription | NHEK | skin |
| 4 | chr6:37362200-37368600 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 5 | chr6:37362800-37368600 | Enhancers | Placenta | Placenta |
| 6 | chr6:37362800-37374000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 7 | chr6:37363800-37373800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 8 | chr6:37363800-37374000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 9 | chr6:37364800-37368600 | Enhancers | Primary neutrophils fromperipheralblood | blood |
| 10 | chr6:37366600-37369800 | Enhancers | K562 | blood |
| 11 | chr6:37368200-37368800 | Enhancers | Right Atrium | heart |
| 12 | chr6:37368400-37368600 | Enhancers | Fetal Intestine Large | intestine |
| 13 | chr6:37368400-37368600 | Enhancers | Gastric | stomach |
| 14 | chr6:37368400-37368600 | Enhancers | Pancreas | Pancrea |
