| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42456960-42457350 | Common:1; Rare:89 | ||||
| chr15:42490222-42490906 | Common:6; Rare:248 | ||||
| chr15:42490957-42491368 | Common:6; Rare:502 | ||||
| chr15:42495028-42495206 | Rare:49 | ||||
| chr15:42495409-42495926 | Common:16; Rare:559 | ||||
| chr15:42495931-42496331 | Rare:100 | ||||
| chr15:42547953-42548678 | Common:4; Rare:386 | ||||
| chr15:42548688-42548937 | Common:13; Rare:639 | ||||
| chr15:42549174-42549363 | Common:1; Rare:84 | ||||
| chr15:42575086-42575289 | Common:2; Rare:93 | ||||
| chr15:42575290-42575740 | Common:14; Rare:589 | ||||
| chr15:42575783-42576183 | Common:2; Rare:105 | ||||
| chr15:42736516-42737399 | Common:12; Rare:984; Clinvar:22; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:42920741-42921141 | Common:8; Rare:344; Clinvar:4 | ||||
| chr15:43105182-43105850 | Common:1; Rare:133 |