Variant report
Variant | rs8021513 |
---|---|
Chromosome Location | chr14:77943007-77943008 |
allele | A/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:77936000-77944600 | Weak transcription | GM12878-XiMat | blood |
2 | chr14:77936200-77948600 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
3 | chr14:77936400-77944800 | Weak transcription | Primary B cells from peripheral blood | blood |
4 | chr14:77936400-77945000 | Weak transcription | Gastric | stomach |
5 | chr14:77936400-77946000 | Weak transcription | Brain Angular Gyrus | brain |
6 | chr14:77936600-77947200 | Weak transcription | Foreskin Melanocyte Primary Cells skin03 | Skin |
7 | chr14:77936800-77945000 | Weak transcription | Primary monocytes fromperipheralblood | blood |
8 | chr14:77937000-77945000 | Weak transcription | Spleen | Spleen |
9 | chr14:77940600-77948600 | Weak transcription | Fetal Kidney | kidney |
10 | chr14:77940800-77945400 | Strong transcription | HepG2 | liver |
11 | chr14:77942400-77944800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
12 | chr14:77942400-77949000 | Weak transcription | Placenta | Placenta |