| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:41962004-41962572 | Common:9; Rare:141 | ||||
| chr3:42149094-42149290 | Rare:45 | ||||
| chr3:42160063-42160221 | Common:1; Rare:33 | ||||
| chr3:42581900-42582206 | Common:3; Rare:90 | ||||
| chr3:42590671-42590965 | Common:3; Rare:89 | ||||
| chr3:42600365-42600778 | Common:2; Rare:158 | ||||
| chr3:42600870-42601046 | Rare:61 | ||||
| chr3:42804260-42804677 | Common:2; Rare:115 | ||||
| chr3:42936326-42936446 | Common:1; Rare:33 | ||||
| chr3:43286459-43286650 | Common:2; Rare:85 | ||||
| chr3:43621919-43622322 | Common:2; Rare:118; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:43690811-43690986 | Common:2; Rare:92; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:43691556-43691643 | Common:1; Rare:14 | ||||
| chr3:44338059-44338169 | Common:2; Rare:38 | ||||
| chr3:44338297-44338477 | Common:2; Rare:61 |