| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12562255-12562577 | Common:3; Rare:78 | ||||
| chr12:12611654-12612113 | Common:2; Rare:132 | ||||
| chr12:12717244-12717646 | Common:1; Rare:128; Clinvar:3; Clinvar (benign):4 | ||||
| chr12:12717649-12718221 | Common:2; Rare:229; Clinvar:41; Clinvar (benign):30; Clinvar (pathogenic):3 | ||||
| chr12:12725642-12726010 | Common:3; Rare:82 | ||||
| chr12:12891294-12891663 | Common:1; Rare:70 | ||||
| chr12:13000204-13000484 | Common:2; Rare:91 | ||||
| chr12:14365927-14366079 | Rare:42 | ||||
| chr12:14385159-14385382 | Rare:42 | ||||
| chr12:14567599-14567638 | Common:3; Rare:19 | ||||
| chr12:14567650-14567982 | Common:2; Rare:76 | ||||
| chr12:14770020-14770079 | Rare:10 | ||||
| chr12:14770930-14771264 | Common:2; Rare:160 | ||||
| chr12:14774184-14774752 | Common:3; Rare:172 | ||||
| chr12:14802956-14803087 | Common:3; Rare:31 |