| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62603500-62603609 | Common:1; Rare:29 | ||||
| chr12:65882083-65882355 | Common:1; Rare:58 | ||||
| chr12:68835717-68835928 | Rare:50 | ||||
| chr12:69252815-69253110 | Common:1; Rare:57 | ||||
| chr12:77324888-77325032 | Common:1; Rare:53 | ||||
| chr12:84911176-84911458 | Common:2; Rare:49 | ||||
| chr12:91183694-91183778 | Rare:17 | ||||
| chr12:95733371-95733581 | Common:1; Rare:28 | ||||
| chr12:103931238-103931564 | Common:1; Rare:60 | ||||
| chr12:103946614-103946941 | Rare:85 | ||||
| chr12:104864575-104864892 | Common:2; Rare:44 | ||||
| chr12:105197874-105198048 | Common:1; Rare:54 | ||||
| chr12:109110938-109111220 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:120291900-120292193 | Common:8; Rare:115 | ||||
| chr12:121931610-121931837 | Rare:59 |