Variant report
| Variant | rs73073547 |
|---|---|
| Chromosome Location | chr2:211425965-211425966 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr2:211418600-211443200 | Weak transcription | H9 Derived Neuronal Progenitor Cultured Cells | ES cell derived |
| 2 | chr2:211422600-211427800 | Weak transcription | Fetal Kidney | kidney |
| 3 | chr2:211423000-211426000 | Weak transcription | ES-I3 Cell Line | embryonic stem cell |
| 4 | chr2:211423600-211432600 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
| 5 | chr2:211423800-211428600 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |
| 6 | chr2:211423800-211432600 | Weak transcription | H9 Cell Line | embryonic stem cell |
| 7 | chr2:211425400-211426200 | Enhancers | Fetal Intestine Small | intestine |
| 8 | chr2:211425400-211426800 | Flanking Active TSS | Liver | Liver |
| 9 | chr2:211425600-211426400 | Genic enhancers | Fetal Intestine Large | intestine |
| 10 | chr2:211425800-211426000 | Enhancers | Duodenum Mucosa | Duodenum |
| 11 | chr2:211425800-211426000 | Flanking Active TSS | Hela-S3 | cervix |
