Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:66366490-66366727 | Common:3; Rare:52 | ||||
chr16:66552476-66552668 | Rare:82 | ||||
chr16:66933675-66934081 | Common:2; Rare:104 | ||||
chr16:66934279-66934515 | Common:1; Rare:88 | ||||
chr16:66988357-66988713 | Common:1; Rare:62 | ||||
chr16:67028933-67029145 | Rare:81 | ||||
chr16:67159885-67159988 | Rare:18 | ||||
chr16:67170434-67170563 | Common:1; Rare:20 | ||||
chr16:67183931-67184011 | Common:1; Rare:26 | ||||
chr16:67227008-67227175 | Rare:68 | ||||
chr16:67247447-67247767 | Common:1; Rare:93 | ||||
chr16:67393092-67393224 | Rare:19 | ||||
chr16:67481074-67481389 | Common:1; Rare:117 | ||||
chr16:67528698-67528899 | Rare:55 | ||||
chr16:67660228-67660379 | Rare:89; Clinvar:2; Clinvar (benign):2 |