| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:16762-17048 | Common:9; Rare:84 | ||||
| chr12:754024-754186 | Rare:58; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:2176732-2176807 | Rare:14 | ||||
| chr12:2274543-2274826 | Rare:51 | ||||
| chr12:2627686-2627954 | Common:5; Rare:50 | ||||
| chr12:2643521-2643738 | Common:2; Rare:41 | ||||
| chr12:5045687-5045754 | Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6769931-6770168 | Common:2; Rare:66 | ||||
| chr12:6770172-6770675 | Rare:132 | ||||
| chr12:6927575-6927801 | Rare:57 | ||||
| chr12:6934170-6934555 | Common:1; Rare:104 | ||||
| chr12:6935443-6935676 | Common:1; Rare:60; Clinvar:1 | ||||
| chr12:7089286-7089746 | Common:3; Rare:148 | ||||
| chr12:8242940-8243235 | Common:8; Rare:84 | ||||
| chr12:9069745-9070076 | Rare:82 |