| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:69239418-69239645 | Common:2; Rare:95 | ||||
| chr12:69348254-69348586 | Common:2; Rare:110; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:69359678-69359811 | Common:3; Rare:51 | ||||
| chr12:69359900-69360317 | Common:10; Rare:238 | ||||
| chr12:69470242-69470446 | Common:6; Rare:155 | ||||
| chr12:69585308-69585507 | Common:6; Rare:161 | ||||
| chr12:70242720-70243120 | Common:4; Rare:157 | ||||
| chr12:70243645-70243770 | Common:2; Rare:68 | ||||
| chr12:71438850-71439300 | Common:2; Rare:135 | ||||
| chr12:71439628-71439994 | Common:6; Rare:118 | ||||
| chr12:71440038-71440256 | Common:1; Rare:78 | ||||
| chr12:71662945-71663440 | Rare:304 | ||||
| chr12:71663633-71664071 | Common:3; Rare:206 | ||||
| chr12:71664130-71664590 | Common:1; Rare:157 | ||||
| chr12:71686023-71686210 | Common:2; Rare:90 |