Variant report
Variant | rs9717400 |
---|---|
Chromosome Location | chr6:88464205-88464206 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:88456400-88465400 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
2 | chr6:88457800-88482400 | Weak transcription | Placenta | Placenta |
3 | chr6:88458200-88465600 | Weak transcription | HepG2 | liver |
4 | chr6:88461800-88466000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
5 | chr6:88462800-88466200 | Weak transcription | Right Atrium | heart |
6 | chr6:88463200-88465600 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
7 | chr6:88463200-88465800 | Weak transcription | NHLF | lung |
8 | chr6:88463400-88465600 | Weak transcription | NHDF-Ad | bronchial |
9 | chr6:88464000-88464600 | Enhancers | Monocytes-CD14+_RO01746 | blood |
10 | chr6:88464000-88469800 | Enhancers | Primary monocytes fromperipheralblood | blood |