| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55927763-55928078 | Rare:91 | ||||
| chr12:55931880-55932095 | Rare:54 | ||||
| chr12:55997056-55997339 | Common:1; Rare:82; Clinvar:2 | ||||
| chr12:56007617-56007836 | Common:2; Rare:50 | ||||
| chr12:56041614-56041968 | Common:4; Rare:83; Clinvar (benign):1 | ||||
| chr12:56104367-56104679 | Common:5; Rare:111 | ||||
| chr12:56116551-56116806 | Common:2; Rare:96 | ||||
| chr12:56152460-56152642 | Rare:55 | ||||
| chr12:56157289-56157482 | Rare:52 | ||||
| chr12:56158015-56158421 | Common:1; Rare:121 | ||||
| chr12:56189438-56189734 | Common:1; Rare:96 | ||||
| chr12:56221669-56222026 | Common:2; Rare:86 | ||||
| chr12:56224228-56224494 | Common:1; Rare:73 | ||||
| chr12:56258301-56258511 | Common:1; Rare:69 | ||||
| chr12:56300006-56300170 | Common:2; Rare:63 |