| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:546665-547103 | Common:5; Rare:105 | ||||
| chr12:642738-643016 | Common:3; Rare:81 | ||||
| chr12:753863-754300 | Common:2; Rare:147; Clinvar:7; Clinvar (benign):5 | ||||
| chr12:926559-926798 | Common:2; Rare:42 | ||||
| chr12:1354479-1354665 | Common:1; Rare:31 | ||||
| chr12:1581771-1582051 | Rare:55 | ||||
| chr12:1936568-1936779 | Common:2; Rare:46 | ||||
| chr12:1966658-1966960 | Common:1; Rare:49 | ||||
| chr12:2244125-2244229 | Common:1; Rare:17 | ||||
| chr12:2799566-2799866 | Rare:58 | ||||
| chr12:2800169-2800577 | Common:1; Rare:86 | ||||
| chr12:3211914-3211925 | Common:1; Rare:2 | ||||
| chr12:3211934-3212035 | Common:6; Rare:18 | ||||
| chr12:4282555-4282807 | Rare:49 | ||||
| chr12:6123498-6123612 | Rare:25 |