Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:69298786-69298946 | Common:3; Rare:34 | ||||
chr15:69414191-69414319 | Rare:31 | ||||
chr15:69452783-69453020 | Common:5; Rare:107 | ||||
chr15:70892363-70892474 | Rare:29 | ||||
chr15:72118167-72118425 | Common:2; Rare:81 | ||||
chr15:72272520-72272657 | Rare:40 | ||||
chr15:72375957-72376137 | Common:2; Rare:74; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr15:72686149-72686220 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
chr15:72783485-72783768 | Common:1; Rare:112 | ||||
chr15:73633265-73633576 | Common:2; Rare:111 | ||||
chr15:73994587-73994792 | Rare:44 | ||||
chr15:74173601-74173754 | Rare:33 | ||||
chr15:74461106-74461338 | Rare:69 | ||||
chr15:74540966-74541268 | Common:3; Rare:107 | ||||
chr15:74695968-74696058 | Rare:32 |