Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:70763437-70763720 | Common:2; Rare:95 | ||||
chr15:71547216-71547311 | Rare:21 | ||||
chr15:72118168-72118403 | Common:2; Rare:74 | ||||
chr15:72231120-72231546 | Common:3; Rare:140 | ||||
chr15:72375957-72376118 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr15:72686129-72686220 | Common:2; Rare:33; Clinvar:2; Clinvar (benign):2 | ||||
chr15:73926265-73926479 | Rare:53 | ||||
chr15:73994600-73994795 | Rare:42 | ||||
chr15:74461106-74461309 | Rare:63 | ||||
chr15:74695973-74696152 | Rare:52 | ||||
chr15:74781898-74782086 | Common:3; Rare:60 | ||||
chr15:74873307-74873440 | Common:5; Rare:45 | ||||
chr15:74889981-74890066 | Rare:34 | ||||
chr15:74995392-74995615 | Common:5; Rare:90 | ||||
chr15:75335967-75336084 | Common:1; Rare:49 |