Variant report
| Variant | rs62174632 |
|---|---|
| Chromosome Location | chr2:173799626-173799627 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:173796400-173800400 | Weak transcription | Fetal Stomach | stomach |
| 2 | chr2:173796400-173802600 | Weak transcription | Duodenum Mucosa | Duodenum |
| 3 | chr2:173796600-173799800 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 4 | chr2:173796600-173800200 | Weak transcription | Fetal Intestine Large | intestine |
| 5 | chr2:173796600-173802800 | Weak transcription | Pancreas | Pancrea |
| 6 | chr2:173796600-173809000 | Weak transcription | Fetal Heart | heart |
| 7 | chr2:173797200-173800400 | Weak transcription | Brain Dorsolateral Prefrontal Cortex | brain |
| 8 | chr2:173798400-173805200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 9 | chr2:173799400-173800200 | Enhancers | Liver | Liver |
| 10 | chr2:173799600-173800600 | Strong transcription | Cortex derived primary cultured neurospheres | brain |
