| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67521075-67521417 | Common:5; Rare:151 | ||||
| chr15:67542604-67542756 | Common:2; Rare:50 | ||||
| chr15:68365206-68365357 | Common:2; Rare:29 | ||||
| chr15:68817407-68817701 | Common:1; Rare:93 | ||||
| chr15:68820709-68821090 | Rare:113 | ||||
| chr15:69298793-69298955 | Common:3; Rare:36 | ||||
| chr15:69452652-69453020 | Common:5; Rare:155 | ||||
| chr15:70892386-70892595 | Common:1; Rare:49 | ||||
| chr15:72117956-72118448 | Common:5; Rare:169 | ||||
| chr15:72231111-72231272 | Rare:61 | ||||
| chr15:72375958-72376137 | Common:2; Rare:74; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:73926322-73926486 | Rare:46 | ||||
| chr15:73994587-73994767 | Rare:36 | ||||
| chr15:74174306-74174572 | Common:3; Rare:50 | ||||
| chr15:74461107-74461314 | Rare:64 |