| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15427414-15427641 | Common:1; Rare:73 | ||||
| chr3:15601447-15601810 | Common:4; Rare:152; Clinvar:2 | ||||
| chr3:15601816-15602046 | Common:1; Rare:117; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr3:15756484-15756644 | Common:2; Rare:30 | ||||
| chr3:15795885-15796083 | Common:3; Rare:30 | ||||
| chr3:15796472-15797044 | Common:5; Rare:109 | ||||
| chr3:15797052-15797545 | Common:6; Rare:102 | ||||
| chr3:15797618-15798037 | Common:3; Rare:76 | ||||
| chr3:15859782-15860170 | Common:5; Rare:117 | ||||
| chr3:15860177-15860230 | Rare:13 | ||||
| chr3:16264818-16265243 | Common:2; Rare:149 | ||||
| chr3:17742513-17742974 | Common:4; Rare:165 | ||||
| chr3:19946989-19947457 | Common:6; Rare:172 | ||||
| chr3:20186129-20186418 | Common:4; Rare:92 | ||||
| chr3:23202926-23203359 | Common:1; Rare:137 |