Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr15:70892361-70892880 | Common:1; Rare:123 | ||||
chr15:71547212-71547285 | Rare:15 | ||||
chr15:72118165-72118435 | Common:2; Rare:89 | ||||
chr15:72231101-72231432 | Common:3; Rare:105 | ||||
chr15:72375944-72376135 | Common:2; Rare:80; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
chr15:72474178-72474354 | Rare:64 | ||||
chr15:72686089-72686220 | Common:2; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
chr15:73633208-73633446 | Common:1; Rare:101 | ||||
chr15:73752225-73752340 | Rare:30 | ||||
chr15:73994600-73994795 | Rare:42 | ||||
chr15:74128192-74128305 | Rare:24 | ||||
chr15:74130073-74130392 | Rare:70 | ||||
chr15:74130447-74130658 | Common:2; Rare:42 | ||||
chr15:74461106-74461307 | Rare:63 | ||||
chr15:74540966-74541293 | Common:4; Rare:118 |