| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:79690520-79690639 | Rare:31 | ||||
| chr12:79690970-79691237 | Common:1; Rare:94 | ||||
| chr12:79934907-79935349 | Common:1; Rare:173 | ||||
| chr12:79935351-79935360 | Rare:2 | ||||
| chr12:82358279-82358556 | Common:1; Rare:130 | ||||
| chr12:82358727-82358889 | Common:3; Rare:83 | ||||
| chr12:88142047-88142394 | Rare:97; Clinvar:3 | ||||
| chr12:89352492-89352672 | Rare:44 | ||||
| chr12:89525998-89526083 | Rare:32 | ||||
| chr12:91111401-91111602 | Common:3; Rare:47 | ||||
| chr12:93441880-93442408 | Common:8; Rare:183 | ||||
| chr12:93571755-93571890 | Common:6; Rare:51 | ||||
| chr12:93677275-93677381 | Rare:22 | ||||
| chr12:94459832-94459994 | Common:2; Rare:45 | ||||
| chr12:95003605-95003831 | Common:3; Rare:94; Clinvar (benign):6 |