| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12717242-12717496 | Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725642-12725997 | Common:3; Rare:80 | ||||
| chr12:13000204-13000476 | Common:2; Rare:89 | ||||
| chr12:13044264-13044403 | Rare:30 | ||||
| chr12:13980567-13980993 | Common:1; Rare:101 | ||||
| chr12:13981524-13981717 | Common:2; Rare:32 | ||||
| chr12:13981882-13982348 | Common:4; Rare:103 | ||||
| chr12:14384997-14385343 | Rare:66 | ||||
| chr12:14774184-14774431 | Common:2; Rare:62 | ||||
| chr12:14803449-14803736 | Common:1; Rare:77 | ||||
| chr12:15221413-15221547 | Common:1; Rare:46 | ||||
| chr12:15322414-15322754 | Rare:104 | ||||
| chr12:15789267-15789548 | Common:1; Rare:93 | ||||
| chr12:15882265-15882435 | Rare:67 | ||||
| chr12:16604923-16605124 | Common:1; Rare:52 |