Variant report
| Variant | rs8097937 |
|---|---|
| Chromosome Location | chr18:29998156-29998157 |
| allele | C/T |
| 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 | chr18:29987800-29998200 | Weak transcription | Left Ventricle | heart |
| 5 | chr18:29990000-29999400 | Weak transcription | Fetal Heart | heart |
| 6 | chr18:29993600-30000200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 7 | chr18:29995800-29999200 | Weak transcription | Brain Anterior Caudate | brain |
| 8 | chr18:29996400-29998800 | Weak transcription | Brain Cingulate Gyrus | brain |
| 9 | chr18:29996400-30000800 | Weak transcription | Brain Inferior Temporal Lobe | brain |
| 10 | chr18:29996600-29998600 | Weak transcription | Brain Hippocampus Middle | brain |
| 11 | chr18:29997200-29999800 | Weak transcription | Adipose Nuclei | Adipose |
| 12 | chr18:29997400-29999800 | Weak transcription | Fetal Lung | lung |
| 13 | chr18:29997800-30002200 | Weak transcription | Fetal Intestine Large | intestine |
| 14 | chr18:29998000-29999000 | Enhancers | HepG2 | liver |
