| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:40224612-40224778 | Rare:39 | ||||
| chr12:40224823-40225168 | Common:5; Rare:104; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:40225177-40225430 | Common:1; Rare:68; Clinvar (benign):1 | ||||
| chr12:40225482-40225646 | Common:1; Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:40225665-40225885 | Common:2; Rare:48 | ||||
| chr12:42325996-42326215 | Common:1; Rare:70 | ||||
| chr12:43758749-43759054 | Common:2; Rare:82; Clinvar:2 | ||||
| chr12:43806220-43806385 | Common:2; Rare:54 | ||||
| chr12:45215970-45216333 | Common:2; Rare:112 | ||||
| chr12:45729379-45729736 | Common:1; Rare:96 | ||||
| chr12:45922490-45922795 | Rare:56 | ||||
| chr12:45990419-45990973 | Common:3; Rare:177 | ||||
| chr12:46268720-46269200 | Common:1; Rare:129 | ||||
| chr12:46371315-46371559 | Common:2; Rare:111 | ||||
| chr12:46372674-46372963 | Rare:121 |