| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:31073776-31073890 | Rare:45 | ||||
| chr12:31326097-31326467 | Common:4; Rare:125 | ||||
| chr12:31729066-31729290 | Common:1; Rare:62 | ||||
| chr12:31959282-31959482 | Common:2; Rare:62 | ||||
| chr12:32755878-32756017 | Rare:46 | ||||
| chr12:32896748-32897062 | Common:4; Rare:101; Clinvar:4; Clinvar (benign):4 | ||||
| chr12:38905580-38905732 | Common:3; Rare:42 | ||||
| chr12:42326011-42326189 | Common:1; Rare:56 | ||||
| chr12:43758746-43758996 | Common:2; Rare:69; Clinvar:2 | ||||
| chr12:45215993-45216154 | Rare:53 | ||||
| chr12:46372755-46373065 | Common:1; Rare:116 | ||||
| chr12:47079521-47079629 | Common:1; Rare:22 | ||||
| chr12:47079676-47079765 | Rare:21 | ||||
| chr12:47705970-47706082 | Rare:51 | ||||
| chr12:48350796-48351159 | Common:7; Rare:129 |