| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67105271-67105397 | Common:2; Rare:17 | ||||
| chr15:67112157-67112457 | Common:12; Rare:35 | ||||
| chr15:67118826-67119204 | Common:1; Rare:64 | ||||
| chr15:67135321-67135498 | Common:1; Rare:31 | ||||
| chr15:67147017-67147154 | Common:1; Rare:41 | ||||
| chr15:67160661-67160964 | Common:3; Rare:39 | ||||
| chr15:67161613-67161797 | Rare:36 | ||||
| chr15:67170555-67170843 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:67171210-67171472 | Rare:53 | ||||
| chr15:67174991-67175141 | Rare:28 | ||||
| chr15:67181240-67181764 | Common:5; Rare:123; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):6 | ||||
| chr15:67187967-67188127 | Common:1; Rare:25 | ||||
| chr15:67196809-67197030 | Common:1; Rare:47 | ||||
| chr15:68101984-68102217 | Common:2; Rare:50 | ||||
| chr15:68121108-68121161 | Rare:6 |