| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51269637-51269811 | Common:1; Rare:43 | ||||
| chr12:51269821-51270350 | Common:5; Rare:178 | ||||
| chr12:51270352-51270462 | Common:1; Rare:29 | ||||
| chr12:51270464-51270604 | Common:5; Rare:34 | ||||
| chr12:51270760-51271021 | Common:3; Rare:37 | ||||
| chr12:51271038-51271136 | Rare:10 | ||||
| chr12:51391029-51391234 | Rare:32 | ||||
| chr12:51391276-51391530 | Common:2; Rare:58 | ||||
| chr12:51391575-51391939 | Common:3; Rare:94 | ||||
| chr12:51392482-51392863 | Common:3; Rare:87 | ||||
| chr12:51424645-51424943 | Common:2; Rare:71 | ||||
| chr12:51425087-51425382 | Rare:60 | ||||
| chr12:51590720-51590974 | Common:1; Rare:74 | ||||
| chr12:51591193-51591328 | Rare:49; Clinvar:3 | ||||
| chr12:51663035-51663129 | Rare:25; Clinvar:1; Clinvar (benign):1 |