| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57111802-57111935 | Common:1; Rare:22 | ||||
| chr12:57128332-57128872 | Common:1; Rare:101 | ||||
| chr12:57128941-57128988 | Rare:9 | ||||
| chr12:57201514-57201862 | Common:2; Rare:81 | ||||
| chr12:57229551-57229753 | Common:3; Rare:84 | ||||
| chr12:57230007-57230228 | Rare:45 | ||||
| chr12:57430724-57431095 | Common:2; Rare:97 | ||||
| chr12:57431147-57431204 | Common:3; Rare:27 | ||||
| chr12:57477812-57478151 | Rare:76 | ||||
| chr12:57504082-57504260 | Rare:49; Clinvar (benign):1 | ||||
| chr12:57517089-57517253 | Rare:45 | ||||
| chr12:57520437-57520727 | Common:2; Rare:86 | ||||
| chr12:57522552-57522901 | Common:3; Rare:133 | ||||
| chr12:57522903-57522993 | Common:1; Rare:20 | ||||
| chr12:57524755-57525027 | Common:1; Rare:91 |