| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6752932-6753178 | Common:6; Rare:72 | ||||
| chr12:6851902-6852195 | Rare:77 | ||||
| chr12:6867409-6867561 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873282-6873546 | Common:2; Rare:76 | ||||
| chr12:6914457-6914612 | Rare:45 | ||||
| chr12:6970602-6970957 | Common:3; Rare:109 | ||||
| chr12:7060390-7060874 | Rare:96 | ||||
| chr12:7092382-7092720 | Rare:74 | ||||
| chr12:7108448-7108695 | Common:1; Rare:71 | ||||
| chr12:7109105-7109532 | Common:1; Rare:109 | ||||
| chr12:7130264-7130425 | Common:4; Rare:44 | ||||
| chr12:7189620-7189733 | Rare:47; Clinvar:4 | ||||
| chr12:8032572-8032777 | Common:4; Rare:69 | ||||
| chr12:8662628-8662876 | Common:4; Rare:51 | ||||
| chr12:8697794-8698116 | Common:2; Rare:117 |