Variant report
| Variant | rs4244192 |
|---|---|
| Chromosome Location | chr1:172072635-172072636 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr1:172040600-172076600 | Weak transcription | Brain Angular Gyrus | brain |
| 2 | chr1:172046600-172076800 | Weak transcription | Fetal Brain Female | brain |
| 3 | chr1:172048000-172083800 | Weak transcription | Aorta | Aorta |
| 4 | chr1:172049400-172110800 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
| 5 | chr1:172052400-172091600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 6 | chr1:172057800-172074000 | Weak transcription | Fetal Lung | lung |
| 7 | chr1:172062400-172074000 | Weak transcription | Fetal Kidney | kidney |
| 8 | chr1:172062400-172109200 | Weak transcription | Brain Cingulate Gyrus | brain |
| 9 | chr1:172069200-172076400 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 10 | chr1:172069200-172102000 | Weak transcription | Brain Hippocampus Middle | brain |
