Variant report
| Variant | rs1621920 |
|---|---|
| Chromosome Location | chr1:61469612-61469613 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:61456400-61471400 | Weak transcription | Fetal Brain Female | brain |
| 2 | chr1:61458200-61477600 | Weak transcription | Left Ventricle | heart |
| 3 | chr1:61460800-61469800 | Weak transcription | K562 | blood |
| 4 | chr1:61466000-61470000 | Weak transcription | Placenta | Placenta |
| 5 | chr1:61466200-61470000 | Weak transcription | Brain Germinal Matrix | brain |
| 6 | chr1:61466600-61470000 | Weak transcription | Fetal Muscle Leg | muscle |
| 7 | chr1:61466600-61478800 | Weak transcription | Skeletal Muscle Male | skeletal muscle |
| 8 | chr1:61469000-61471600 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
| 9 | chr1:61469200-61471600 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
| 10 | chr1:61469400-61470600 | Bivalent Enhancer | H1 Cell Line | embryonic stem cell |
| 11 | chr1:61469600-61470600 | Enhancers | Primary monocytes fromperipheralblood | blood |
| 12 | chr1:61469600-61470600 | Enhancers | Monocytes-CD14+_RO01746 | blood |
| 13 | chr1:61469600-61471400 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
