Variant report
Variant | rs3127663 |
---|---|
Chromosome Location | chr6:107147266-107147267 |
allele | C/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr6:107136000-107148200 | Weak transcription | H9 Cell Line | embryonic stem cell |
2 | chr6:107141200-107148200 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
3 | chr6:107142000-107147600 | Weak transcription | iPS-18 Cell Line | embryonic stem cell |
4 | chr6:107142600-107148200 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
5 | chr6:107142600-107157400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
6 | chr6:107142800-107148200 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
7 | chr6:107146000-107147400 | Enhancers | Pancreas | Pancrea |
8 | chr6:107146200-107147400 | Weak transcription | Primary B cells from cord blood | blood |
9 | chr6:107146400-107149200 | Weak transcription | Primary hematopoietic stem cells | blood |
10 | chr6:107147000-107150000 | Enhancers | Primary B cells from peripheral blood | blood |
11 | chr6:107147200-107150000 | Weak transcription | Primary neutrophils fromperipheralblood | blood |