Variant report
| Variant | rs34661013 |
|---|---|
| Chromosome Location | chr2:209420777-209420778 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:209418200-209420800 | Weak transcription | K562 | blood |
| 2 | chr2:209418200-209421600 | Weak transcription | Fetal Heart | heart |
| 3 | chr2:209419600-209424000 | Weak transcription | Fetal Intestine Small | intestine |
| 4 | chr2:209420200-209421600 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
