| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120437754-120438229 | Common:6; Rare:396; Clinvar (benign):5 | ||||
| chr12:120446270-120446541 | Common:8; Rare:281 | ||||
| chr12:120463696-120464180 | Common:3; Rare:164 | ||||
| chr12:120469016-120469416 | Common:6; Rare:249 | ||||
| chr12:120469423-120470003 | Common:15; Rare:459 | ||||
| chr12:120495804-120496240 | Common:21; Rare:368 | ||||
| chr12:120529049-120529275 | Common:5; Rare:141 | ||||
| chr12:120534223-120534451 | Common:1; Rare:107 | ||||
| chr12:120534720-120535613 | Common:4; Rare:542 | ||||
| chr12:120581257-120581623 | Common:4; Rare:340 | ||||
| chr12:120640410-120640730 | Rare:74 | ||||
| chr12:120686265-120686615 | Common:3; Rare:93 | ||||
| chr12:120686640-120686860 | Rare:93 | ||||
| chr12:120686859-120687251 | Common:5; Rare:319 | ||||
| chr12:120687220-120688013 | Common:2; Rare:259 |