| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55725928-55726259 | Rare:79 | ||||
| chr12:55726890-55727333 | Common:2; Rare:146 | ||||
| chr12:55728286-55728742 | Rare:118 | ||||
| chr12:55728816-55729141 | Common:2; Rare:69 | ||||
| chr12:55729516-55729809 | Common:1; Rare:61 | ||||
| chr12:55829500-55829804 | Rare:95 | ||||
| chr12:55830729-55830919 | Rare:63 | ||||
| chr12:55927763-55928069 | Rare:86 | ||||
| chr12:55966704-55966980 | Rare:73 | ||||
| chr12:56041563-56041984 | Common:4; Rare:88; Clinvar (benign):1 | ||||
| chr12:56152440-56152625 | Rare:58 | ||||
| chr12:56158223-56158432 | Rare:73 | ||||
| chr12:56315823-56316224 | Common:2; Rare:98 | ||||
| chr12:56350746-56350857 | Rare:18 | ||||
| chr12:56642515-56642696 | Rare:46 |