| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32755884-32755959 | Rare:31 | ||||
| chr12:32896764-32896976 | Common:1; Rare:70; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:38905584-38905810 | Common:5; Rare:66 | ||||
| chr12:42238186-42238562 | Common:4; Rare:122 | ||||
| chr12:42326008-42326218 | Common:1; Rare:69 | ||||
| chr12:43758749-43758991 | Common:2; Rare:66; Clinvar:2 | ||||
| chr12:43806237-43806412 | Common:2; Rare:60 | ||||
| chr12:44875582-44875705 | Common:2; Rare:29 | ||||
| chr12:44876054-44876459 | Common:3; Rare:128 | ||||
| chr12:45215996-45216154 | Rare:52 | ||||
| chr12:46267310-46267438 | Rare:28 | ||||
| chr12:47705962-47706099 | Rare:61 | ||||
| chr12:48004490-48004855 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chr12:48105839-48105948 | Rare:28 | ||||
| chr12:48106014-48106062 | Rare:11 |