| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:95003627-95003806 | Common:3; Rare:73; Clinvar (benign):4 | ||||
| chr12:95217427-95217886 | Common:3; Rare:122 | ||||
| chr12:95858822-95859037 | Common:2; Rare:58 | ||||
| chr12:96035547-96035743 | Common:2; Rare:43 | ||||
| chr12:96907174-96907285 | Rare:41 | ||||
| chr12:98515428-98515767 | Rare:113; Clinvar:2 | ||||
| chr12:99154712-99154854 | Rare:30 | ||||
| chr12:99154865-99154995 | Rare:30 | ||||
| chr12:99984172-99984412 | Rare:51 | ||||
| chr12:100200553-100200863 | Common:3; Rare:91 | ||||
| chr12:100266979-100267326 | Common:2; Rare:157 | ||||
| chr12:100573601-100573700 | Rare:23 | ||||
| chr12:101280027-101280143 | Common:1; Rare:35 | ||||
| chr12:101407731-101408035 | Common:2; Rare:73 | ||||
| chr12:102061934-102062193 | Common:1; Rare:74 |