| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15205945-15206300 | Common:2; Rare:239 | ||||
| chr3:15332521-15332677 | Common:4; Rare:96 | ||||
| chr3:15427454-15427641 | Common:2; Rare:125 | ||||
| chr3:15601491-15601838 | Common:9; Rare:278; Clinvar:6; Clinvar (benign):1 | ||||
| chr3:15601859-15602048 | Common:1; Rare:97; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:15858789-15859106 | Common:1; Rare:67 | ||||
| chr3:15859420-15859710 | Common:18; Rare:150 | ||||
| chr3:15859725-15860176 | Common:9; Rare:256 | ||||
| chr3:16264881-16265279 | Common:6; Rare:255 | ||||
| chr3:16884886-16885018 | Rare:31 | ||||
| chr3:17741860-17742480 | Common:2; Rare:281 | ||||
| chr3:17742499-17742963 | Common:8; Rare:310 | ||||
| chr3:19946871-19947451 | Common:19; Rare:407 | ||||
| chr3:20040124-20040447 | Common:5; Rare:85 | ||||
| chr3:20186074-20186482 | Common:8; Rare:198 |