Variant report
| Variant | rs2953060 |
|---|---|
| Chromosome Location | chr11:16086747-16086748 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr11:16024800-16088200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 2 | chr11:16043000-16102000 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 3 | chr11:16068800-16103800 | Weak transcription | Left Ventricle | heart |
| 4 | chr11:16074800-16092200 | Weak transcription | Fetal Intestine Small | intestine |
| 5 | chr11:16075200-16092600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
| 6 | chr11:16083200-16116000 | Weak transcription | Fetal Intestine Large | intestine |
| 7 | chr11:16083600-16096400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 8 | chr11:16086400-16088200 | Enhancers | Primary neutrophils fromperipheralblood | blood |
