| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42273749-42274280 | Common:1; Rare:105 | ||||
| chr15:42274406-42274501 | Rare:26 | ||||
| chr15:42490605-42490814 | Common:2; Rare:38 | ||||
| chr15:42490933-42491319 | Common:1; Rare:102 | ||||
| chr15:42491595-42491802 | Rare:41 | ||||
| chr15:42495036-42495219 | Rare:33 | ||||
| chr15:42495380-42495859 | Common:2; Rare:114 | ||||
| chr15:42548275-42548406 | Rare:40 | ||||
| chr15:42548415-42549310 | Common:5; Rare:271 | ||||
| chr15:42575087-42575371 | Common:1; Rare:83 | ||||
| chr15:42575387-42575763 | Common:3; Rare:128 | ||||
| chr15:42736485-42736559 | Common:1; Rare:21; Clinvar (benign):1 | ||||
| chr15:42736922-42737331 | Common:1; Rare:154; Clinvar:3 | ||||
| chr15:42919929-42920014 | Common:2; Rare:18 | ||||
| chr15:42920610-42920623 | Common:1; Rare:4; Clinvar (benign):1 |