| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:4648496-4648858 | Common:5; Rare:63 | ||||
| chr12:4648941-4649178 | Common:2; Rare:75; Clinvar (benign):2 | ||||
| chr12:4649270-4649359 | Rare:17 | ||||
| chr12:5431953-5432142 | Common:4; Rare:74 | ||||
| chr12:5945191-5945418 | Common:1; Rare:84 | ||||
| chr12:6199966-6200098 | Rare:38 | ||||
| chr12:6200113-6200441 | Common:4; Rare:95 | ||||
| chr12:6201229-6201388 | Common:2; Rare:36 | ||||
| chr12:6310033-6310459 | Common:2; Rare:88 | ||||
| chr12:6310468-6310789 | Common:4; Rare:90 | ||||
| chr12:6310915-6311052 | Common:2; Rare:43 | ||||
| chr12:6311127-6311348 | Common:3; Rare:63 | ||||
| chr12:6312514-6312682 | Common:1; Rare:37 | ||||
| chr12:6312721-6312932 | Common:2; Rare:25 | ||||
| chr12:6313003-6313236 | Common:2; Rare:55 |