| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57694198-57694321 | Common:1; Rare:28 | ||||
| chr12:57769373-57769643 | Common:2; Rare:87; Clinvar:1 | ||||
| chr12:57771586-57771863 | Common:1; Rare:65 | ||||
| chr12:57772031-57772286 | Rare:94 | ||||
| chr12:57772506-57772634 | Common:2; Rare:20 | ||||
| chr12:57782918-57783223 | Common:2; Rare:96; Clinvar (benign):2 | ||||
| chr12:57824617-57824768 | Rare:31 | ||||
| chr12:58920491-58920642 | Common:2; Rare:55 | ||||
| chr12:62260165-62260495 | Common:1; Rare:122 | ||||
| chr12:62578320-62578431 | Rare:19 | ||||
| chr12:63779994-63780150 | Common:1; Rare:73; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr12:63843562-63844000 | Common:5; Rare:124 | ||||
| chr12:63844384-63844816 | Rare:102 | ||||
| chr12:64222232-64222349 | Rare:43 | ||||
| chr12:64404226-64404649 | Common:5; Rare:154 |