Variant report
Variant | rs72825628 |
---|---|
Chromosome Location | chr6:15893040-15893041 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:15883400-15895800 | Weak transcription | Esophagus | oesophagus |
2 | chr6:15889600-15897200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin02 | Skin |
3 | chr6:15889600-15897400 | Weak transcription | Spleen | Spleen |
4 | chr6:15889800-15895800 | Weak transcription | Fetal Lung | lung |
5 | chr6:15890200-15897200 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
6 | chr6:15892000-15893400 | Enhancers | Monocytes-CD14+_RO01746 | blood |
7 | chr6:15892000-15893600 | Enhancers | Primary monocytes fromperipheralblood | blood |
8 | chr6:15892800-15894400 | Weak transcription | Placenta | Placenta |
9 | chr6:15893000-15897200 | Weak transcription | Right Atrium | heart |