| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41283708-41284069 | Common:3; Rare:102 | ||||
| chr15:41490340-41490630 | Common:7; Rare:38 | ||||
| chr15:41558233-41558496 | Common:1; Rare:38 | ||||
| chr15:41603810-41604490 | Common:4; Rare:124 | ||||
| chr15:41862879-41863009 | Common:1; Rare:32 | ||||
| chr15:41933840-41934160 | Common:4; Rare:60 | ||||
| chr15:42057052-42057154 | Common:1; Rare:27 | ||||
| chr15:42057231-42057399 | Common:1; Rare:36 | ||||
| chr15:42057526-42057734 | Common:1; Rare:47 | ||||
| chr15:42092210-42092690 | Common:1; Rare:83 | ||||
| chr15:42118770-42119260 | Common:11; Rare:94 | ||||
| chr15:42385596-42385727 | Rare:42 | ||||
| chr15:42401645-42401876 | Rare:80; Clinvar:10; Clinvar (benign):1; Clinvar (pathogenic):10 | ||||
| chr15:42581573-42581676 | Common:1; Rare:32 | ||||
| chr15:44102921-44103251 | Common:1; Rare:62 |