Variant report
Variant | rs2239264 |
---|---|
Chromosome Location | chr14:72561999-72562000 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr14:72556800-72563400 | Weak transcription | Left Ventricle | heart |
2 | chr14:72556800-72563400 | Weak transcription | Right Atrium | heart |
3 | chr14:72558400-72563600 | Weak transcription | Fetal Muscle Leg | muscle |
4 | chr14:72560200-72562200 | Enhancers | Brain Germinal Matrix | brain |
5 | chr14:72560600-72566600 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |
6 | chr14:72560800-72562200 | Enhancers | Cortex derived primary cultured neurospheres | brain |
7 | chr14:72561200-72564000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
8 | chr14:72561400-72562000 | Enhancers | Fetal Brain Male | brain |
9 | chr14:72561400-72562400 | Enhancers | Fetal Brain Female | brain |
10 | chr14:72561400-72562600 | Flanking Active TSS | GM12878-XiMat | blood |
11 | chr14:72561600-72562000 | Enhancers | Right Ventricle | heart |
12 | chr14:72561800-72562400 | Active TSS | Primary T regulatory cells fromperipheralblood | blood |