| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:23039495-23039773 | Common:1; Rare:117 | ||||
| chr15:23566239-23566343 | Rare:57; Clinvar (pathogenic):1 | ||||
| chr15:23647836-23648194 | Common:2; Rare:85 | ||||
| chr15:23687219-23687498 | Common:1; Rare:98 | ||||
| chr15:24823560-24823790 | Common:1; Rare:52; Clinvar:1 | ||||
| chr15:24856455-24856687 | Common:2; Rare:57 | ||||
| chr15:24954831-24954994 | Common:1; Rare:67 | ||||
| chr15:25438285-25438491 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr15:25438920-25439285 | Common:3; Rare:130 | ||||
| chr15:25863090-25863660 | Common:5; Rare:138 | ||||
| chr15:26772950-26773330 | Common:2; Rare:147; Clinvar (benign):1 | ||||
| chr15:26773673-26774150 | Common:5; Rare:178; Clinvar:1; Clinvar (benign):5 | ||||
| chr15:26866950-26867094 | Common:3; Rare:36 | ||||
| chr15:26867651-26868051 | Common:1; Rare:100 | ||||
| chr15:26970835-26971235 | Common:1; Rare:118 |