Variant report
| Variant | rs10184942 |
|---|---|
| Chromosome Location | chr2:48634787-48634788 |
| allele | A/C |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:48628200-48640000 | Weak transcription | Brain Inferior Temporal Lobe | brain |
| 2 | chr2:48632200-48635000 | Enhancers | Fetal Intestine Large | intestine |
| 3 | chr2:48632200-48635200 | Enhancers | Fetal Intestine Small | intestine |
| 4 | chr2:48634000-48641400 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 5 | chr2:48634400-48641800 | Weak transcription | Brain Dorsolateral Prefrontal Cortex | brain |
| 6 | chr2:48634600-48635400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 7 | chr2:48634600-48640200 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 8 | chr2:48634600-48641400 | Weak transcription | Duodenum Mucosa | Duodenum |
| 9 | chr2:48634600-48642200 | Weak transcription | Small Intestine | intestine |
