| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44729609-44729658 | Rare:7 | ||||
| chr15:45023033-45023385 | Common:3; Rare:105 | ||||
| chr15:45023483-45023618 | Rare:30 | ||||
| chr15:45129832-45130097 | Rare:56 | ||||
| chr15:45187927-45188106 | Common:2; Rare:71 | ||||
| chr15:45200437-45200818 | Common:2; Rare:112 | ||||
| chr15:45201033-45201190 | Common:3; Rare:60 | ||||
| chr15:45378215-45378293 | Rare:14 | ||||
| chr15:45378342-45378365 | Rare:5 | ||||
| chr15:45402148-45402499 | Common:6; Rare:116; Clinvar:1 | ||||
| chr15:45402510-45402899 | Common:3; Rare:149 | ||||
| chr15:45522315-45522390 | Rare:29 | ||||
| chr15:45522517-45522609 | Rare:19 | ||||
| chr15:45522680-45522891 | Common:1; Rare:63 | ||||
| chr15:45587018-45587633 | Common:2; Rare:172; Clinvar:7; Clinvar (benign):3 |