Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:99733378-99733633 | Common:10; Rare:85 | ||||
chr15:100602167-100602506 | Common:3; Rare:87 | ||||
chr15:101277408-101277625 | Common:3; Rare:115 | ||||
chr15:101295133-101295375 | Rare:73 | ||||
chr16:53549-53911 | Common:7; Rare:127 | ||||
chr16:397112-397312 | Common:4; Rare:52 | ||||
chr16:1771530-1771604 | Rare:32 | ||||
chr16:1782510-1783012 | Common:4; Rare:165 | ||||
chr16:1827179-1827232 | Rare:29 | ||||
chr16:1943165-1943513 | Common:1; Rare:109 | ||||
chr16:1964814-1965061 | Common:6; Rare:111 | ||||
chr16:1971893-1972110 | Common:1; Rare:62 | ||||
chr16:2047795-2048038 | Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2268066-2268187 | Common:1; Rare:59 | ||||
chr16:2513622-2514011 | Rare:135 |