| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6752940-6753236 | Common:10; Rare:156 | ||||
| chr12:6753420-6753800 | Common:8; Rare:145 | ||||
| chr12:6765550-6765860 | Common:2; Rare:73 | ||||
| chr12:6765891-6766652 | Common:3; Rare:302 | ||||
| chr12:6766941-6767170 | Common:3; Rare:53 | ||||
| chr12:6851232-6851508 | Rare:126 | ||||
| chr12:6851879-6852203 | Rare:165 | ||||
| chr12:6855761-6857048 | Common:12; Rare:434 | ||||
| chr12:6867355-6867673 | Common:4; Rare:211; Clinvar:2; Clinvar (benign):4 | ||||
| chr12:6867889-6868867 | Common:25; Rare:510 | ||||
| chr12:6873274-6873674 | Common:6; Rare:194 | ||||
| chr12:6904676-6904855 | Rare:41 | ||||
| chr12:6914280-6914620 | Rare:149 | ||||
| chr12:6924369-6924498 | Common:1; Rare:29 | ||||
| chr12:6927369-6927908 | Rare:147 |