| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12611765-12612179 | Common:3; Rare:121 | ||||
| chr12:12717798-12717874 | Rare:33; Clinvar:7; Clinvar (benign):3 | ||||
| chr12:12785541-12785660 | Rare:21 | ||||
| chr12:12891364-12891567 | Common:1; Rare:36 | ||||
| chr12:13000074-13000489 | Common:2; Rare:126 | ||||
| chr12:14567673-14567963 | Common:2; Rare:66 | ||||
| chr12:14771087-14771157 | Common:1; Rare:47 | ||||
| chr12:14774184-14774752 | Common:3; Rare:172 | ||||
| chr12:14803451-14803680 | Common:1; Rare:56 | ||||
| chr12:15882261-15882666 | Common:1; Rare:131 | ||||
| chr12:21501565-21501835 | Common:1; Rare:66 | ||||
| chr12:21941219-21941293 | Rare:14 | ||||
| chr12:21941305-21941325 | Rare:5 | ||||
| chr12:22334650-22335007 | Common:1; Rare:109 | ||||
| chr12:22544144-22544284 | Rare:68 |