| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103965717-103965941 | Common:2; Rare:51 | ||||
| chr12:104064465-104064586 | Rare:32 | ||||
| chr12:104286729-104287065 | Common:3; Rare:63 | ||||
| chr12:104287208-104287346 | Rare:34 | ||||
| chr12:104288756-104288968 | Rare:93 | ||||
| chr12:105107612-105107789 | Common:1; Rare:80 | ||||
| chr12:105236049-105236286 | Common:2; Rare:103 | ||||
| chr12:106955527-106955796 | Rare:92 | ||||
| chr12:106987040-106987278 | Common:4; Rare:69 | ||||
| chr12:107685717-107685940 | Rare:72 | ||||
| chr12:108515013-108515313 | Common:1; Rare:92 | ||||
| chr12:108562439-108562731 | Common:9; Rare:125; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108731456-108731638 | Common:2; Rare:66 | ||||
| chr12:109052515-109052653 | Common:2; Rare:45 | ||||
| chr12:109116147-109116442 | Common:5; Rare:53 |