Variant report
Variant | rs12665472 |
---|---|
Chromosome Location | chr6:107305068-107305069 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:107300400-107305400 | Weak transcription | Foreskin Keratinocyte Primary Cells skin03 | Skin |
2 | chr6:107300600-107307200 | Weak transcription | Esophagus | oesophagus |
3 | chr6:107302000-107305800 | Weak transcription | Small Intestine | intestine |
4 | chr6:107302800-107306200 | Weak transcription | Primary neutrophils fromperipheralblood | blood |
5 | chr6:107303200-107307000 | Enhancers | K562 | blood |
6 | chr6:107304400-107305600 | Weak transcription | HMEC | breast |
7 | chr6:107304600-107306000 | Weak transcription | Stomach Mucosa | stomach |
8 | chr6:107304600-107306400 | Weak transcription | Osteobl | bone |