Variant report
Variant | rs60797189 |
---|---|
Chromosome Location | chr2:171620651-171620652 |
allele | A/G |
Outlinks | Ensembl   UCSC |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr2:171574000-171620800 | Weak transcription | Pancreas | Pancrea |
2 | chr2:171613200-171626800 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
3 | chr2:171618600-171626600 | Weak transcription | Primary T cells effector/memory enriched fromperipheralblood | blood |
4 | chr2:171619600-171626800 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
5 | chr2:171620600-171620800 | Enhancers | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
6 | chr2:171620600-171621400 | Enhancers | K562 | blood |
7 | chr2:171620600-171622200 | Enhancers | Ganglion Eminence derived primary cultured neurospheres | brain |