| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32399271-32399607 | Common:4; Rare:86 | ||||
| chr12:32399842-32399949 | Rare:30 | ||||
| chr12:32896760-32896990 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:38905548-38905648 | Common:3; Rare:30 | ||||
| chr12:39619785-39620110 | Common:2; Rare:53 | ||||
| chr12:42238187-42238483 | Rare:102 | ||||
| chr12:42326032-42326207 | Common:1; Rare:58 | ||||
| chr12:43758749-43759021 | Common:2; Rare:76; Clinvar:2 | ||||
| chr12:43806229-43806385 | Common:2; Rare:54 | ||||
| chr12:45216007-45216163 | Rare:49 | ||||
| chr12:46268750-46269236 | Common:1; Rare:130 | ||||
| chr12:47079521-47079655 | Common:1; Rare:26 | ||||
| chr12:47705972-47706107 | Rare:62 | ||||
| chr12:47758148-47758270 | Common:1; Rare:22 | ||||
| chr12:47758836-47759027 | Common:1; Rare:39 |