| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:100266941-100267462 | Common:4; Rare:220 | ||||
| chr12:100267808-100267917 | Common:1; Rare:23 | ||||
| chr12:100573545-100573733 | Rare:65 | ||||
| chr12:100573879-100573935 | Common:2; Rare:19 | ||||
| chr12:101279994-101280386 | Common:1; Rare:114 | ||||
| chr12:101407458-101407535 | Rare:20 | ||||
| chr12:101407702-101408149 | Common:3; Rare:113 | ||||
| chr12:101697434-101697916 | Common:4; Rare:154 | ||||
| chr12:101830600-101830661 | Common:2; Rare:18; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:101830728-101831169 | Common:2; Rare:139; Clinvar (benign):2 | ||||
| chr12:101877111-101877981 | Common:9; Rare:221 | ||||
| chr12:102061693-102062206 | Common:2; Rare:139 | ||||
| chr12:102119984-102120276 | Common:1; Rare:115 | ||||
| chr12:102120431-102120568 | Common:2; Rare:40 | ||||
| chr12:102917238-102917416 | Common:2; Rare:52; Clinvar (benign):1 |