| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6723821-6724289 | Common:1; Rare:103 | ||||
| chr12:6752923-6753223 | Common:6; Rare:91 | ||||
| chr12:6766504-6766741 | Rare:66 | ||||
| chr12:6789417-6789588 | Rare:38 | ||||
| chr12:6851245-6851486 | Rare:56 | ||||
| chr12:6867353-6867562 | Common:2; Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873320-6873659 | Common:3; Rare:97 | ||||
| chr12:6943911-6944172 | Common:10; Rare:261; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6970418-6970961 | Common:3; Rare:168 | ||||
| chr12:7018431-7018488 | Rare:25 | ||||
| chr12:7108459-7108709 | Common:1; Rare:69 | ||||
| chr12:7130240-7130440 | Common:5; Rare:54 | ||||
| chr12:7189563-7189738 | Rare:64; Clinvar:4 | ||||
| chr12:8032613-8032764 | Rare:52 | ||||
| chr12:8697742-8698043 | Common:1; Rare:121 |