| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:2864378-2864725 | Common:4; Rare:99 | ||||
| chr12:2876935-2877285 | Rare:115 | ||||
| chr12:2890702-2890977 | Common:1; Rare:108 | ||||
| chr12:2959329-2959484 | Common:1; Rare:42 | ||||
| chr12:2959813-2959980 | Common:1; Rare:44 | ||||
| chr12:3873331-3873514 | Common:1; Rare:42 | ||||
| chr12:4273636-4274037 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr12:4320949-4321300 | Common:5; Rare:136 | ||||
| chr12:4538426-4538947 | Common:3; Rare:123 | ||||
| chr12:4648960-4649178 | Common:2; Rare:71; Clinvar (benign):2 | ||||
| chr12:4763593-4763813 | Common:3; Rare:45 | ||||
| chr12:4809198-4809363 | Rare:36 | ||||
| chr12:5431934-5432130 | Common:4; Rare:79 | ||||
| chr12:6200059-6200565 | Common:4; Rare:153 | ||||
| chr12:6310528-6310773 | Common:4; Rare:59 |