Variant report
| Variant | rs72716989 |
|---|---|
| Chromosome Location | chr1:85261949-85261950 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:85241000-85263600 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr1:85251800-85263400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 3 | chr1:85261200-85262200 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 4 | chr1:85261200-85262200 | Enhancers | Primary hematopoietic stem cells short term culture | blood |
| 5 | chr1:85261400-85262000 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 6 | chr1:85261400-85262400 | Enhancers | Fetal Adrenal Gland | Adrenal Gland |
| 7 | chr1:85261600-85262200 | Enhancers | HepG2 | liver |
| 8 | chr1:85261600-85262800 | Weak transcription | Fetal Heart | heart |
| 9 | chr1:85261600-85263000 | Weak transcription | Esophagus | oesophagus |
| 10 | chr1:85261600-85263000 | Weak transcription | Left Ventricle | heart |
| 11 | chr1:85261600-85263400 | Active TSS | Right Atrium | heart |
