| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109900159-109900391 | Rare:77 | ||||
| chr12:109996299-109996439 | Common:2; Rare:39 | ||||
| chr12:109999099-109999217 | Rare:18 | ||||
| chr12:110124157-110124462 | Common:1; Rare:103 | ||||
| chr12:110281012-110281209 | Rare:73 | ||||
| chr12:110403608-110403751 | Common:2; Rare:81 | ||||
| chr12:110450235-110450458 | Common:2; Rare:79 | ||||
| chr12:110468648-110468924 | Rare:76 | ||||
| chr12:110502051-110502331 | Common:1; Rare:101 | ||||
| chr12:110613996-110614242 | Rare:78; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110689138-110689460 | Common:1; Rare:68 | ||||
| chr12:110742783-110743197 | Common:3; Rare:149 | ||||
| chr12:111599283-111599668 | Common:3; Rare:136 | ||||
| chr12:111685737-111686127 | Rare:141 | ||||
| chr12:111766785-111766980 | Rare:60 |