Variant report
| Variant | rs61915685 |
|---|---|
| Chromosome Location | chr12:26252548-26252549 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr12:26244600-26254200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 2 | chr12:26245200-26254000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 3 | chr12:26250400-26253000 | Weak transcription | Fetal Intestine Small | intestine |
| 4 | chr12:26250600-26254000 | Weak transcription | Stomach Mucosa | stomach |
| 5 | chr12:26250600-26254200 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 6 | chr12:26250800-26254000 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 7 | chr12:26250800-26254000 | Weak transcription | HMEC | breast |
| 8 | chr12:26251000-26254000 | Weak transcription | NHEK | skin |
| 9 | chr12:26251000-26265800 | Weak transcription | HSMM | muscle |
| 10 | chr12:26252400-26255800 | Enhancers | Fetal Intestine Large | intestine |
