Variant report
| Variant | rs17073445 |
|---|---|
| Chromosome Location | chr13:50407477-50407478 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:50396000-50414400 | Weak transcription | Right Atrium | heart |
| 2 | chr13:50402200-50412800 | Weak transcription | Fetal Intestine Small | intestine |
| 3 | chr13:50403000-50410200 | Weak transcription | HepG2 | liver |
| 4 | chr13:50404000-50410600 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
| 5 | chr13:50405800-50414200 | Weak transcription | Primary hematopoietic stem cells | blood |
| 6 | chr13:50406000-50410400 | Weak transcription | Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells | embryonic stem cell |
| 7 | chr13:50407200-50407600 | Enhancers | K562 | blood |
| 8 | chr13:50407200-50407800 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
| 9 | chr13:50407400-50407800 | Enhancers | HUES6 Cell Line | embryonic stem cell |
| 10 | chr13:50407400-50407800 | Enhancers | iPS-20b Cell Line | embryonic stem cell |
| 11 | chr13:50407400-50407800 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
| 12 | chr13:50407400-50408000 | Enhancers | Esophagus | oesophagus |
