Variant report
| Variant | rs7993059 |
|---|---|
| Chromosome Location | chr13:50419702-50419703 |
| allele | A/T |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:50411400-50422000 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 2 | chr13:50413000-50421600 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
| 3 | chr13:50415000-50420600 | Weak transcription | K562 | blood |
| 4 | chr13:50415400-50421600 | Weak transcription | HepG2 | liver |
| 5 | chr13:50415400-50421800 | Weak transcription | Fetal Adrenal Gland | Adrenal Gland |
| 6 | chr13:50415600-50421800 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 7 | chr13:50417600-50421800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
| 8 | chr13:50418800-50421800 | Weak transcription | Foreskin Fibroblast Primary Cells skin01 | Skin |
| 9 | chr13:50418800-50421800 | Weak transcription | Foreskin Fibroblast Primary Cells skin02 | Skin |
| 10 | chr13:50418800-50421800 | Weak transcription | NHDF-Ad | bronchial |
| 11 | chr13:50419600-50419800 | Enhancers | Primary mononuclear cells fromperipheralblood | Blood |
