| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:63151028-63151311 | Common:2; Rare:50 | ||||
| chr12:63668444-63668761 | Common:4; Rare:88 | ||||
| chr12:63780085-63780143 | Rare:24; Clinvar (pathogenic):1 | ||||
| chr12:64222259-64222369 | Rare:27 | ||||
| chr12:64452014-64452174 | Common:1; Rare:59 | ||||
| chr12:64610569-64610604 | Rare:15 | ||||
| chr12:64759161-64759501 | Common:1; Rare:108; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65278590-65278833 | Common:1; Rare:89; Clinvar (benign):3 | ||||
| chr12:66130718-66130805 | Rare:29 | ||||
| chr12:68332265-68332615 | Common:1; Rare:115 | ||||
| chr12:68610704-68611050 | Common:1; Rare:144 | ||||
| chr12:68686825-68687034 | Common:4; Rare:63 | ||||
| chr12:69470280-69470450 | Common:3; Rare:70 | ||||
| chr12:69585308-69585506 | Common:3; Rare:80 | ||||
| chr12:70242877-70243039 | Common:1; Rare:60 |