Variant report
Variant | rs607735 |
---|---|
Chromosome Location | chr6:36541545-36541546 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:36535000-36546400 | Weak transcription | Fetal Intestine Large | intestine |
2 | chr6:36535000-36546800 | Weak transcription | Primary B cells from cord blood | blood |
3 | chr6:36535200-36551200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
4 | chr6:36540000-36547800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
5 | chr6:36540200-36542000 | Enhancers | Placenta | Placenta |
6 | chr6:36541000-36542400 | Enhancers | Primary neutrophils fromperipheralblood | blood |
7 | chr6:36541000-36544600 | Weak transcription | Fetal Intestine Small | intestine |
8 | chr6:36541400-36542800 | Weak transcription | HepG2 | liver |
9 | chr6:36541400-36544400 | Weak transcription | IMR90 fetal lung fibroblasts Cell Line | lung |
10 | chr6:36541400-36544400 | Weak transcription | A549 | lung |
11 | chr6:36541400-36544400 | Weak transcription | Hela-S3 | cervix |