Variant report
| Variant | rs186188663 |
|---|---|
| Chromosome Location | chr1:210628259-210628260 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:210571400-210641000 | Weak transcription | Duodenum Smooth Muscle | Duodenum |
| 2 | chr1:210611600-210639600 | Weak transcription | Aorta | Aorta |
| 3 | chr1:210614600-210641200 | Weak transcription | Gastric | stomach |
| 4 | chr1:210620200-210637800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 5 | chr1:210622000-210630800 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
| 6 | chr1:210622400-210631600 | Weak transcription | HSMM | muscle |
| 7 | chr1:210625800-210638800 | Weak transcription | Breast Myoepithelial Primary Cells | Breast |
| 8 | chr1:210626200-210650000 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 9 | chr1:210626400-210628400 | Strong transcription | HSMMtube | muscle |
| 10 | chr1:210627400-210630800 | Weak transcription | Fetal Kidney | kidney |
| 11 | chr1:210628000-210629200 | Enhancers | Dnd41 | blood |
