Variant report
| Variant | rs61409769 |
|---|---|
| Chromosome Location | chr1:213561414-213561415 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:213555400-213567000 | Weak transcription | Right Atrium | heart |
| 2 | chr1:213556200-213561600 | Weak transcription | Left Ventricle | heart |
| 3 | chr1:213556800-213561600 | Weak transcription | Fetal Muscle Trunk | muscle |
| 4 | chr1:213558000-213573600 | Enhancers | HepG2 | liver |
| 5 | chr1:213558600-213564400 | Weak transcription | Fetal Heart | heart |
| 6 | chr1:213561000-213563400 | Enhancers | Fetal Lung | lung |
| 7 | chr1:213561200-213561800 | Bivalent Enhancer | Cortex derived primary cultured neurospheres | brain |
| 8 | chr1:213561200-213561800 | Enhancers | Spleen | Spleen |
| 9 | chr1:213561200-213562600 | Enhancers | Brain Germinal Matrix | brain |
| 10 | chr1:213561400-213562400 | Enhancers | Brain Anterior Caudate | brain |
| 11 | chr1:213561400-213563000 | Enhancers | iPS DF 19.11 Cell Line | embryonic stem cell |
