Variant report
Variant | rs1513961 |
---|---|
Chromosome Location | chr11:18138476-18138477 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr11:18129000-18139000 | Weak transcription | Right Atrium | heart |
2 | chr11:18136600-18141600 | Enhancers | HepG2 | liver |
3 | chr11:18136800-18139800 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
4 | chr11:18136800-18141600 | Enhancers | Breast Myoepithelial Primary Cells | Breast |
5 | chr11:18137400-18141600 | Enhancers | Foreskin Melanocyte Primary Cells skin03 | Skin |
6 | chr11:18138200-18140200 | Enhancers | Foreskin Melanocyte Primary Cells skin01 | Skin |
7 | chr11:18138400-18139200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |