| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:12287734-12287970 | Common:6; Rare:47 | ||||
| chr3:12556863-12557135 | Common:5; Rare:85 | ||||
| chr3:12664084-12664298 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:13480029-13480324 | Common:2; Rare:72 | ||||
| chr3:14124742-14125144 | Common:4; Rare:116; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:14178564-14178870 | Common:2; Rare:160; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:14651468-14651807 | Rare:99 | ||||
| chr3:14947283-14947574 | Common:3; Rare:132 | ||||
| chr3:15206008-15206269 | Rare:93 | ||||
| chr3:15427470-15427618 | Common:1; Rare:56 | ||||
| chr3:15601519-15601815 | Common:4; Rare:125; Clinvar:2 | ||||
| chr3:15797157-15797368 | Common:6; Rare:47 | ||||
| chr3:16264878-16265243 | Common:2; Rare:120 | ||||
| chr3:19946853-19947450 | Common:10; Rare:219 | ||||
| chr3:20186161-20186415 | Common:2; Rare:81 |