| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44663513-44663952 | Rare:182; Clinvar:13; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr15:44676837-44676894 | Rare:12 | ||||
| chr15:44710734-44711093 | Common:3; Rare:54 | ||||
| chr15:44711110-44711665 | Common:1; Rare:143; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711832-44711989 | Rare:31 | ||||
| chr15:44712157-44712185 | Rare:5 | ||||
| chr15:44712589-44712741 | Rare:44 | ||||
| chr15:44728628-44729239 | Common:1; Rare:115 | ||||
| chr15:44729459-44729602 | Common:2; Rare:31 | ||||
| chr15:44736252-44736561 | Common:3; Rare:64 | ||||
| chr15:45023031-45023255 | Common:3; Rare:56 | ||||
| chr15:45187941-45188148 | Common:3; Rare:77 | ||||
| chr15:45200490-45200713 | Common:1; Rare:59 | ||||
| chr15:45201052-45201138 | Common:2; Rare:32 | ||||
| chr15:45378342-45378666 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):12 |