| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7108438-7108671 | Common:1; Rare:72 | ||||
| chr12:7109203-7109367 | Rare:46 | ||||
| chr12:7189544-7189750 | Common:1; Rare:76; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:8697742-8698014 | Common:1; Rare:110 | ||||
| chr12:9732960-9733025 | Common:1; Rare:20 | ||||
| chr12:9760754-9761018 | Common:2; Rare:51 | ||||
| chr12:9869248-9869482 | Common:1; Rare:34 | ||||
| chr12:9869615-9869915 | Common:4; Rare:59 | ||||
| chr12:10613540-10613725 | Common:1; Rare:74 | ||||
| chr12:11171597-11171708 | Common:1; Rare:35 | ||||
| chr12:12356860-12357212 | Common:5; Rare:150 | ||||
| chr12:12611784-12611924 | Common:2; Rare:38 | ||||
| chr12:12696562-12696789 | Rare:63 | ||||
| chr12:12717267-12717486 | Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:12725651-12726071 | Common:4; Rare:106 |