| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50783628-50783842 | Common:1; Rare:63 | ||||
| chr3:9362945-9363091 | Common:2; Rare:55 | ||||
| chr3:9792414-9792480 | Rare:14 | ||||
| chr3:10115503-10115702 | Common:4; Rare:71 | ||||
| chr3:12664087-12664330 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:14124751-14125068 | Common:4; Rare:92; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178569-14178857 | Common:2; Rare:149; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:15427523-15427613 | Rare:30 | ||||
| chr3:23916919-23917173 | Rare:94 | ||||
| chr3:36993190-36993539 | Common:2; Rare:102; Clinvar:25; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr3:39051944-39052031 | Common:1; Rare:32 | ||||
| chr3:44761600-44761810 | Common:3; Rare:73 | ||||
| chr3:44976126-44976264 | Common:2; Rare:58 | ||||
| chr3:47475818-47476078 | Common:3; Rare:106 | ||||
| chr3:48440120-48440303 | Common:1; Rare:72 |