| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23916894-23917214 | Rare:123 | ||||
| chr3:23945125-23945346 | Common:6; Rare:85 | ||||
| chr3:25783391-25783622 | Common:2; Rare:76; Clinvar (benign):3 | ||||
| chr3:28348809-28349158 | Common:2; Rare:110 | ||||
| chr3:29280831-29281095 | Common:3; Rare:52 | ||||
| chr3:36992722-36992886 | Rare:59 | ||||
| chr3:36993102-36993564 | Common:2; Rare:148; Clinvar:27; Clinvar (benign):12; Clinvar (pathogenic):3 | ||||
| chr3:37176233-37176398 | Rare:55 | ||||
| chr3:38137075-38137447 | Common:1; Rare:82 | ||||
| chr3:39051983-39052056 | Common:1; Rare:30 | ||||
| chr3:39107519-39107740 | Common:4; Rare:68 | ||||
| chr3:39383570-39383668 | Rare:19; Clinvar:1 | ||||
| chr3:40309496-40309809 | Common:9; Rare:108 | ||||
| chr3:42581903-42582113 | Common:2; Rare:66 | ||||
| chr3:42582256-42582428 | Common:1; Rare:43 |