| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107760956-107761390 | Common:16; Rare:387 | ||||
| chr12:107774110-107774550 | Common:1; Rare:87 | ||||
| chr12:108129496-108129839 | Common:1; Rare:75 | ||||
| chr12:108514933-108515387 | Common:3; Rare:334 | ||||
| chr12:108561089-108561678 | Common:12; Rare:331 | ||||
| chr12:108562284-108562696 | Common:29; Rare:387; Clinvar:6; Clinvar (benign):12 | ||||
| chr12:108701215-108701895 | Common:1; Rare:137 | ||||
| chr12:108730553-108731116 | Common:5; Rare:217 | ||||
| chr12:108731376-108731750 | Common:8; Rare:301 | ||||
| chr12:108731878-108732367 | Common:7; Rare:202 | ||||
| chr12:108857515-108857933 | Common:5; Rare:404 | ||||
| chr12:109052451-109052776 | Common:9; Rare:189 | ||||
| chr12:109093385-109093683 | Common:7; Rare:282 | ||||
| chr12:109097345-109097693 | Rare:274; Clinvar:7 | ||||
| chr12:109097877-109098301 | Common:14; Rare:321 |