| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123712108-123712497 | Common:8; Rare:142; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:123712573-123712683 | Rare:39; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:123712730-123712757 | Common:1; Rare:4 | ||||
| chr12:123972719-123972848 | Common:2; Rare:50 | ||||
| chr12:123972941-123973323 | Common:2; Rare:121 | ||||
| chr12:123973352-123973509 | Common:2; Rare:32 | ||||
| chr12:123973763-123973827 | Rare:12 | ||||
| chr12:124388809-124388974 | Common:3; Rare:48 | ||||
| chr12:124518253-124518390 | Common:2; Rare:33 | ||||
| chr12:124518546-124518748 | Rare:47 | ||||
| chr12:124567151-124567325 | Common:1; Rare:44 | ||||
| chr12:124567427-124567512 | Rare:17 | ||||
| chr12:124567558-124568114 | Common:5; Rare:167 | ||||
| chr12:124863464-124863515 | Rare:7 | ||||
| chr12:124863637-124863894 | Common:4; Rare:70 |