Variant report
| Variant | rs4647386 |
|---|---|
| Chromosome Location | chr9:98050410-98050411 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr9:98046600-98059400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
| 2 | chr9:98046600-98063000 | Weak transcription | Fetal Stomach | stomach |
| 3 | chr9:98047200-98059400 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 4 | chr9:98047400-98055800 | Weak transcription | HepG2 | liver |
| 5 | chr9:98048000-98055000 | Weak transcription | Fetal Intestine Small | intestine |
| 6 | chr9:98048800-98054400 | Weak transcription | Fetal Intestine Large | intestine |
| 7 | chr9:98048800-98059200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
| 8 | chr9:98049200-98051000 | Weak transcription | Small Intestine | intestine |
| 9 | chr9:98049200-98054400 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
| 10 | chr9:98050000-98059200 | Weak transcription | HSMM | muscle |
| 11 | chr9:98050200-98067400 | Weak transcription | A549 | lung |
