Variant report
| Variant | rs2647441 |
|---|---|
| Chromosome Location | chr1:220136940-220136941 |
| allele | G/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:220129200-220145800 | Weak transcription | HepG2 | liver |
| 2 | chr1:220132000-220138800 | Weak transcription | Aorta | Aorta |
| 3 | chr1:220132200-220144200 | Weak transcription | Primary T killer naive cells fromperipheralblood | blood |
| 4 | chr1:220132400-220143200 | Weak transcription | Colonic Mucosa | Colon |
| 5 | chr1:220132800-220141000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 6 | chr1:220132800-220177000 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 7 | chr1:220133000-220141200 | Weak transcription | Duodenum Mucosa | Duodenum |
| 8 | chr1:220133400-220138600 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 9 | chr1:220133600-220140800 | Weak transcription | Fetal Intestine Large | intestine |
| 10 | chr1:220133600-220141000 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 11 | chr1:220133600-220142200 | Weak transcription | Small Intestine | intestine |
| 12 | chr1:220135400-220137800 | Weak transcription | K562 | blood |
| 13 | chr1:220136400-220138000 | Enhancers | Liver | Liver |
