Variant report
| Variant | rs12988106 |
|---|---|
| Chromosome Location | chr2:11613152-11613153 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:11607000-11621200 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
| 2 | chr2:11607200-11622400 | Weak transcription | Spleen | Spleen |
| 3 | chr2:11607600-11618000 | Weak transcription | Primary T cells from cord blood | blood |
| 4 | chr2:11612000-11613800 | Enhancers | HepG2 | liver |
| 5 | chr2:11612600-11613200 | Active TSS | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
| 6 | chr2:11612600-11613600 | Enhancers | H9 Derived Neuron Cultured Cells | ES cell derived |
| 7 | chr2:11612800-11614800 | Enhancers | Fetal Muscle Leg | muscle |
| 8 | chr2:11613000-11615200 | Enhancers | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
