Variant report
| Variant | rs189096202 |
|---|---|
| Chromosome Location | chr6:143617384-143617385 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr6:143598600-143620200 | Weak transcription | Brain Angular Gyrus | brain |
| 2 | chr6:143603200-143622200 | Weak transcription | Brain Hippocampus Middle | brain |
| 3 | chr6:143605600-143622000 | Weak transcription | HepG2 | liver |
| 4 | chr6:143607600-143622200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 5 | chr6:143608400-143620800 | Weak transcription | Stomach Smooth Muscle | stomach |
| 6 | chr6:143608600-143620800 | Weak transcription | Left Ventricle | heart |
| 7 | chr6:143608600-143624200 | Weak transcription | Aorta | Aorta |
| 8 | chr6:143608800-143619800 | Weak transcription | HMEC | breast |
| 9 | chr6:143608800-143624200 | Weak transcription | Ovary | ovary |
| 10 | chr6:143608800-143629400 | Weak transcription | NHEK | skin |
| 11 | chr6:143609400-143622400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 12 | chr6:143609800-143621000 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
| 13 | chr6:143610000-143626000 | Weak transcription | Fetal Intestine Large | intestine |
| 14 | chr6:143613800-143624400 | Weak transcription | Fetal Intestine Small | intestine |
| 15 | chr6:143615400-143643400 | Weak transcription | HSMM | muscle |
| 16 | chr6:143616400-143618600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 17 | chr6:143616800-143620200 | Weak transcription | Liver | Liver |
| 18 | chr6:143616800-143624400 | Weak transcription | K562 | blood |
| 19 | chr6:143617200-143617400 | Enhancers | Fetal Brain Male | brain |
