Variant report
Variant | rs74063385 |
---|---|
Chromosome Location | chr14:77966859-77966860 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:77965600-77977600 | Weak transcription | Aorta | Aorta |
2 | chr14:77965800-77967200 | Weak transcription | Ganglion Eminence derived primary cultured neurospheres | brain |
3 | chr14:77965800-77974600 | Weak transcription | A549 | lung |
4 | chr14:77966000-77973400 | Weak transcription | Cortex derived primary cultured neurospheres | brain |
5 | chr14:77966000-77977400 | Weak transcription | HMEC | breast |
6 | chr14:77966200-77970600 | Weak transcription | HSMM | muscle |
7 | chr14:77966400-77972800 | Weak transcription | Esophagus | oesophagus |
8 | chr14:77966400-77974000 | Weak transcription | Primary T helper cells fromperipheralblood | blood |
9 | chr14:77966400-77976800 | Weak transcription | Spleen | Spleen |
10 | chr14:77966400-77977000 | Weak transcription | Pancreas | Pancrea |
11 | chr14:77966400-77977600 | Weak transcription | Gastric | stomach |
12 | chr14:77966600-77967200 | Flanking Active TSS | HepG2 | liver |
13 | chr14:77966600-77977000 | Weak transcription | Sigmoid Colon | Sigmoid Colon |
14 | chr14:77966600-77977600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
15 | chr14:77966600-77977800 | Weak transcription | Foreskin Melanocyte Primary Cells skin01 | Skin |
16 | chr14:77966800-77972600 | Weak transcription | Osteobl | bone |
17 | chr14:77966800-77972800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
18 | chr14:77966800-77973200 | Weak transcription | Placenta | Placenta |