| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55973494-55973959 | Common:3; Rare:112 | ||||
| chr12:55973975-55974181 | Common:1; Rare:61 | ||||
| chr12:55974386-55974546 | Rare:34 | ||||
| chr12:55997027-55997384 | Common:2; Rare:95; Clinvar:2 | ||||
| chr12:56007244-56007549 | Common:1; Rare:61 | ||||
| chr12:56007729-56007866 | Common:2; Rare:28 | ||||
| chr12:56041530-56042259 | Common:6; Rare:199; Clinvar:3; Clinvar (benign):6 | ||||
| chr12:56042358-56042578 | Rare:64; Clinvar (benign):1 | ||||
| chr12:56104088-56104705 | Common:6; Rare:205 | ||||
| chr12:56116427-56116794 | Common:3; Rare:146 | ||||
| chr12:56117866-56118339 | Common:1; Rare:146 | ||||
| chr12:56118345-56118633 | Common:1; Rare:45 | ||||
| chr12:56127847-56128432 | Rare:139 | ||||
| chr12:56151735-56152031 | Common:1; Rare:56 | ||||
| chr12:56152119-56152290 | Common:1; Rare:40 |