Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:19718467-19718581 | Rare:40 | ||||
chr16:20676146-20676315 | Common:2; Rare:28 | ||||
chr16:20741551-20741617 | Rare:29 | ||||
chr16:20763924-20764029 | Common:2; Rare:14 | ||||
chr16:20806317-20806495 | Rare:57 | ||||
chr16:20900226-20901099 | Common:6; Rare:203 | ||||
chr16:21158510-21158740 | Common:1; Rare:66 | ||||
chr16:21599390-21599825 | Common:4; Rare:156 | ||||
chr16:21652581-21652911 | Rare:66 | ||||
chr16:21952975-21953452 | Common:1; Rare:121; Clinvar (benign):3 | ||||
chr16:21957259-21957566 | Rare:104; Clinvar (benign):1 | ||||
chr16:22206547-22206581 | Rare:9 | ||||
chr16:22374593-22374835 | Common:1; Rare:79 | ||||
chr16:22436926-22437399 | Rare:157 | ||||
chr16:22437407-22437707 | Common:2; Rare:85 |