Variant report
| Variant | rs58367312 |
|---|---|
| Chromosome Location | chr18:29995487-29995488 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr18:29963600-29999200 | Weak transcription | Fetal Kidney | kidney |
| 2 | chr18:29982000-30005400 | Weak transcription | Stomach Mucosa | stomach |
| 3 | chr18:29987400-29999800 | Weak transcription | Brain Angular Gyrus | brain |
| 4 | chr18:29987800-29995600 | Weak transcription | Brain Hippocampus Middle | brain |
| 5 | chr18:29987800-29998200 | Weak transcription | Left Ventricle | heart |
| 6 | chr18:29990000-29999400 | Weak transcription | Fetal Heart | heart |
| 7 | chr18:29993600-30000200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 8 | chr18:29995200-29996400 | Enhancers | Brain Cingulate Gyrus | brain |
| 9 | chr18:29995400-29995800 | Enhancers | Brain Anterior Caudate | brain |
| 10 | chr18:29995400-29995800 | Enhancers | Brain Substantia Nigra | brain |
| 11 | chr18:29995400-29996400 | Enhancers | Brain Inferior Temporal Lobe | brain |
