| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70892280-70892810 | Common:4; Rare:198 | ||||
| chr15:72118001-72118448 | Common:7; Rare:297 | ||||
| chr15:72118480-72118740 | Common:1; Rare:119 | ||||
| chr15:72231100-72231520 | Common:6; Rare:261 | ||||
| chr15:72375907-72376170 | Common:5; Rare:187; Clinvar:18; Clinvar (benign):4; Clinvar (pathogenic):10 | ||||
| chr15:72474154-72474558 | Rare:247 | ||||
| chr15:72474710-72475100 | Common:3; Rare:167; Clinvar (benign):2 | ||||
| chr15:72686116-72686440 | Common:4; Rare:189; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr15:72783656-72783884 | Common:4; Rare:175 | ||||
| chr15:73052050-73052530 | Common:6; Rare:214 | ||||
| chr15:73633223-73633627 | Common:5; Rare:312 | ||||
| chr15:73684183-73684463 | Rare:155 | ||||
| chr15:73992270-73992540 | Common:3; Rare:109 | ||||
| chr15:73994568-73994810 | Common:2; Rare:97 | ||||
| chr15:74365120-74365820 | Common:5; Rare:144 |