| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107685717-107685939 | Rare:72 | ||||
| chr12:107692834-107693094 | Common:1; Rare:77 | ||||
| chr12:108560838-108560857 | Rare:2 | ||||
| chr12:108561065-108561429 | Common:4; Rare:108 | ||||
| chr12:108731977-108732220 | Common:2; Rare:65 | ||||
| chr12:109477240-109477711 | Common:4; Rare:130 | ||||
| chr12:109573430-109573869 | Common:3; Rare:143; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr12:109880316-109880669 | Common:1; Rare:110 | ||||
| chr12:109899990-109900332 | Common:1; Rare:90 | ||||
| chr12:109999118-109999457 | Rare:77 | ||||
| chr12:110281571-110281917 | Common:1; Rare:98; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr12:110345949-110346182 | Rare:73; Clinvar:2 | ||||
| chr12:110445501-110445629 | Rare:35 | ||||
| chr12:110468665-110468885 | Rare:54 | ||||
| chr12:110502026-110502158 | Common:1; Rare:54 |