Variant report
| Variant | rs11601397 |
|---|---|
| Chromosome Location | chr11:47689718-47689719 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr11:47676800-47703400 | Weak transcription | Fetal Intestine Small | intestine |
| 2 | chr11:47687000-47692600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 3 | chr11:47687200-47693800 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 4 | chr11:47688200-47690400 | Enhancers | Fetal Lung | lung |
| 5 | chr11:47688600-47691000 | Enhancers | HepG2 | liver |
| 6 | chr11:47689000-47694000 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 7 | chr11:47689400-47711200 | Weak transcription | Liver | Liver |
