| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105021031-105021373 | Common:1; Rare:122 | ||||
| chr14:105419733-105420032 | Rare:95 | ||||
| chr14:105487053-105487205 | Common:1; Rare:42 | ||||
| chr15:22786492-22786776 | Rare:105; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:23039529-23039703 | Common:1; Rare:73 | ||||
| chr15:23565481-23565697 | Common:2; Rare:61 | ||||
| chr15:23566214-23566359 | Rare:75; Clinvar (pathogenic):1 | ||||
| chr15:24954650-24955051 | Common:1; Rare:149 | ||||
| chr15:25438984-25439272 | Common:2; Rare:114 | ||||
| chr15:26629044-26629400 | Common:5; Rare:121 | ||||
| chr15:26773746-26773999 | Common:2; Rare:62; Clinvar (benign):1 | ||||
| chr15:30903685-30903970 | Common:2; Rare:72 | ||||
| chr15:31870625-31870953 | Rare:105 | ||||
| chr15:32030344-32030619 | Common:7; Rare:101 | ||||
| chr15:32615091-32615679 | Common:7; Rare:148 |