Variant report
| Variant | rs12798752 |
|---|---|
| Chromosome Location | chr11:16336148-16336149 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr11:16315200-16351800 | Weak transcription | Fetal Intestine Large | intestine |
| 2 | chr11:16319400-16377600 | Weak transcription | Psoas Muscle | Psoas |
| 3 | chr11:16320600-16340600 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 4 | chr11:16327800-16342400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 5 | chr11:16328600-16348400 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
| 6 | chr11:16330600-16344200 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 7 | chr11:16331400-16340000 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
| 8 | chr11:16333800-16356400 | Weak transcription | Fetal Intestine Small | intestine |
