| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8017692-8017888 | Rare:32 | ||||
| chr12:8081124-8081286 | Rare:24 | ||||
| chr12:8653226-8653428 | Common:2; Rare:30 | ||||
| chr12:8687859-8688025 | Rare:33 | ||||
| chr12:8844212-8844255 | Rare:7 | ||||
| chr12:8855503-8855664 | Common:1; Rare:50; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:8872205-8872444 | Common:2; Rare:48 | ||||
| chr12:8875796-8876139 | Common:2; Rare:54 | ||||
| chr12:9240490-9240719 | Common:2; Rare:44 | ||||
| chr12:9447842-9447980 | Common:3; Rare:22 | ||||
| chr12:9448185-9448295 | Common:1; Rare:55 | ||||
| chr12:9689437-9689698 | Common:2; Rare:44 | ||||
| chr12:10379805-10379850 | Common:1; Rare:17 | ||||
| chr12:10708043-10708075 | Rare:4 | ||||
| chr12:10719078-10719372 | Rare:71 |