Variant report
| Variant | rs61453037 |
|---|---|
| Chromosome Location | chr7:150997991-150997992 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr7:150994000-151000400 | Weak transcription | Right Atrium | heart |
| 2 | chr7:150997000-151002000 | Weak transcription | Gastric | stomach |
| 3 | chr7:150997200-150999000 | Weak transcription | Fetal Kidney | kidney |
| 4 | chr7:150997200-151000400 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 5 | chr7:150997200-151000800 | Weak transcription | H1 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 6 | chr7:150997200-151000800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 7 | chr7:150997600-150998000 | Bivalent Enhancer | Foreskin Melanocyte Primary Cells skin01 | Skin |
| 8 | chr7:150997600-151000800 | Weak transcription | Pancreas | Pancrea |
