| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:20186138-20186473 | Common:5; Rare:109 | ||||
| chr3:23916919-23917210 | Rare:110 | ||||
| chr3:25783374-25783641 | Common:2; Rare:90; Clinvar (benign):3 | ||||
| chr3:25790006-25790118 | Common:3; Rare:43 | ||||
| chr3:28348987-28349168 | Common:2; Rare:55 | ||||
| chr3:29280806-29281094 | Common:3; Rare:58 | ||||
| chr3:33798435-33798706 | Common:2; Rare:90 | ||||
| chr3:36993078-36993545 | Common:2; Rare:158; Clinvar:26; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr3:37176091-37176389 | Common:1; Rare:84 | ||||
| chr3:37243229-37243369 | Common:1; Rare:37 | ||||
| chr3:37861709-37861891 | Common:1; Rare:41 | ||||
| chr3:38137087-38137419 | Common:1; Rare:68 | ||||
| chr3:39107500-39107732 | Common:4; Rare:78 | ||||
| chr3:39383289-39383432 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39383582-39383661 | Rare:17; Clinvar:1 |