| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134412472-134412872 | Common:6; Rare:120 | ||||
| chr11:134801800-134802750 | Common:18; Rare:260 | ||||
| chr12:143899-144299 | Common:1; Rare:106 | ||||
| chr12:144314-144607 | Common:2; Rare:84 | ||||
| chr12:188690-189143 | Common:6; Rare:126 | ||||
| chr12:390355-390755 | Rare:71 | ||||
| chr12:402201-402601 | Common:5; Rare:103 | ||||
| chr12:569817-570077 | Common:4; Rare:75 | ||||
| chr12:570354-570754 | Common:3; Rare:88 | ||||
| chr12:576164-576424 | Common:3; Rare:66 | ||||
| chr12:642599-642999 | Common:6; Rare:163 | ||||
| chr12:751191-751504 | Common:1; Rare:80 | ||||
| chr12:753843-754328 | Common:3; Rare:195; Clinvar:10; Clinvar (benign):8 | ||||
| chr12:968421-968737 | Common:2; Rare:40 | ||||
| chr12:968768-969168 | Common:8; Rare:104 |