| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:15065135-15065393 | Common:4; Rare:165 | ||||
| chr3:15098546-15098946 | Rare:85 | ||||
| chr3:15099054-15099479 | Common:2; Rare:210 | ||||
| chr3:15205933-15206366 | Common:3; Rare:372 | ||||
| chr3:15245025-15245587 | Common:1; Rare:121 | ||||
| chr3:15246915-15247046 | Common:1; Rare:19 | ||||
| chr3:15331295-15331710 | Common:9; Rare:114 | ||||
| chr3:15331765-15331941 | Rare:36 | ||||
| chr3:15331987-15332704 | Common:16; Rare:399 | ||||
| chr3:15427414-15427730 | Common:3; Rare:225 | ||||
| chr3:15600997-15601400 | Common:5; Rare:212 | ||||
| chr3:15601433-15602076 | Common:17; Rare:754; Clinvar:14; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr3:15602236-15602405 | Rare:46 | ||||
| chr3:15797883-15798221 | Rare:99 | ||||
| chr3:15858958-15859183 | Common:1; Rare:63 |