Variant report
| Variant | rs70939078 |
|---|---|
| Chromosome Location | chr2:21419519-21419520 |
| allele | -/AT |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:21416200-21421400 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 2 | chr2:21416200-21424400 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
| 3 | chr2:21416600-21420600 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 4 | chr2:21417000-21420200 | Weak transcription | Brain Anterior Caudate | brain |
| 5 | chr2:21417800-21421000 | Enhancers | Brain Substantia Nigra | brain |
| 6 | chr2:21418400-21419600 | Weak transcription | Brain Angular Gyrus | brain |
| 7 | chr2:21418400-21419800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
| 8 | chr2:21418600-21419600 | Weak transcription | Brain Cingulate Gyrus | brain |
| 9 | chr2:21418600-21419600 | Weak transcription | Brain Hippocampus Middle | brain |
| 10 | chr2:21418600-21419800 | Weak transcription | Brain Inferior Temporal Lobe | brain |
| 11 | chr2:21418600-21422800 | Weak transcription | Fetal Intestine Large | intestine |
| 12 | chr2:21419400-21421200 | Enhancers | Fetal Brain Male | brain |
