Variant report
| Variant | rs11886633 |
|---|---|
| Chromosome Location | chr2:209355305-209355306 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:209353200-209356600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 2 | chr2:209353600-209355600 | Enhancers | Fetal Lung | lung |
| 3 | chr2:209354200-209355600 | Enhancers | Colon Smooth Muscle | Colon |
| 4 | chr2:209354400-209357400 | Enhancers | K562 | blood |
| 5 | chr2:209354600-209357600 | Weak transcription | Pancreas | Pancrea |
| 6 | chr2:209355200-209361000 | Weak transcription | Stomach Mucosa | stomach |
| 7 | chr2:209355200-209366000 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
