Variant report
| Variant | rs5998660 |
|---|---|
| Chromosome Location | chr22:33331900-33331901 |
| allele | C/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr22:33314000-33380800 | Weak transcription | iPS DF 6.9 Cell Line | embryonic stem cell |
| 2 | chr22:33314200-33332200 | Weak transcription | HepG2 | liver |
| 3 | chr22:33319200-33333000 | Weak transcription | Fetal Brain Male | brain |
| 4 | chr22:33326600-33332200 | Weak transcription | HUES6 Cell Line | embryonic stem cell |
| 5 | chr22:33327600-33332600 | Weak transcription | iPS-20b Cell Line | embryonic stem cell |
| 6 | chr22:33328600-33335400 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 7 | chr22:33328800-33334600 | Weak transcription | ES-UCSF4 Cell Line | embryonic stem cell |
| 8 | chr22:33329000-33333400 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
| 9 | chr22:33329200-33336000 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
| 10 | chr22:33329400-33333400 | Weak transcription | H1 Cell Line | embryonic stem cell |
| 11 | chr22:33330800-33332200 | Weak transcription | Placenta Amnion | Placenta Amnion |
| 12 | chr22:33331400-33342800 | Weak transcription | Fetal Heart | heart |
