| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:100341862-100342239 | Common:8; Rare:197; Clinvar:10; Clinvar (benign):2 | ||||
| chr15:100602088-100602877 | Common:12; Rare:530 | ||||
| chr15:100603141-100603491 | Common:6; Rare:95 | ||||
| chr15:100879518-100879895 | Common:4; Rare:220 | ||||
| chr15:100918950-100919370 | Common:4; Rare:190 | ||||
| chr15:100919288-100919392 | Rare:33 | ||||
| chr15:100919390-100919850 | Common:9; Rare:201 | ||||
| chr15:101251419-101251850 | Common:12; Rare:294; Clinvar:2 | ||||
| chr15:101251863-101252229 | Common:5; Rare:282 | ||||
| chr15:101252260-101252580 | Common:8; Rare:181 | ||||
| chr15:101277307-101277686 | Common:12; Rare:453 | ||||
| chr15:101293910-101294950 | Common:9; Rare:362 | ||||
| chr15:101295159-101295476 | Common:3; Rare:249 | ||||
| chr15:101489210-101489610 | Common:19; Rare:187 | ||||
| chr15:101489605-101489891 | Common:4; Rare:237 |