Variant report
Variant | rs4666385 |
---|---|
Chromosome Location | chr2:20575321-20575322 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:20565200-20578400 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
2 | chr2:20570200-20578600 | Weak transcription | Ovary | ovary |
3 | chr2:20571800-20576600 | Weak transcription | Fetal Lung | lung |
4 | chr2:20572800-20578400 | Weak transcription | Fetal Brain Male | brain |
5 | chr2:20574800-20575400 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
6 | chr2:20574800-20575400 | Enhancers | Placenta | Placenta |
7 | chr2:20575000-20578600 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
8 | chr2:20575200-20575400 | Bivalent Enhancer | HepG2 | liver |
9 | chr2:20575200-20575800 | Enhancers | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
10 | chr2:20575200-20576800 | Weak transcription | Aorta | Aorta |
11 | chr2:20575200-20578600 | Weak transcription | HUES6 Cell Line | embryonic stem cell |