Variant report
| Variant | rs16844256 |
|---|---|
| Chromosome Location | chr1:172278797-172278798 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:172256200-172290000 | Weak transcription | Brain Hippocampus Middle | brain |
| 2 | chr1:172256400-172290200 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 3 | chr1:172256600-172289800 | Weak transcription | Brain Inferior Temporal Lobe | brain |
| 4 | chr1:172272600-172291600 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 5 | chr1:172275200-172309800 | Weak transcription | Left Ventricle | heart |
| 6 | chr1:172277400-172278800 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 7 | chr1:172277400-172279000 | Enhancers | Fetal Kidney | kidney |
| 8 | chr1:172277400-172279200 | Enhancers | Fetal Lung | lung |
| 9 | chr1:172277400-172279200 | Enhancers | Fetal Stomach | stomach |
