Variant report
Variant | rs10979191 |
---|---|
Chromosome Location | chr9:110845493-110845494 |
allele | C/T |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr9:110828400-110846800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
2 | chr9:110837400-110848800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
3 | chr9:110840400-110848000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
4 | chr9:110841800-110845600 | Weak transcription | Primary monocytes fromperipheralblood | blood |
5 | chr9:110841800-110845600 | Weak transcription | Monocytes-CD14+_RO01746 | blood |
6 | chr9:110845400-110845800 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
7 | chr9:110845400-110846000 | Bivalent Enhancer | Cortex derived primary cultured neurospheres | brain |
8 | chr9:110845400-110846200 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |