| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104138170-104138442 | Common:1; Rare:81 | ||||
| chr12:105107612-105107789 | Common:1; Rare:80 | ||||
| chr12:105236049-105236306 | Common:2; Rare:113 | ||||
| chr12:106987056-106987277 | Common:4; Rare:64 | ||||
| chr12:107685717-107685895 | Rare:63 | ||||
| chr12:108562393-108562662 | Common:8; Rare:113; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:109097847-109098214 | Common:5; Rare:116 | ||||
| chr12:109477287-109477653 | Common:3; Rare:90 | ||||
| chr12:109573470-109573837 | Common:3; Rare:108; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:109880381-109880664 | Common:1; Rare:86 | ||||
| chr12:109900177-109900332 | Rare:59 | ||||
| chr12:109996313-109996439 | Common:2; Rare:35 | ||||
| chr12:110468671-110468909 | Rare:59 | ||||
| chr12:110502051-110502226 | Common:1; Rare:62 | ||||
| chr12:111685761-111686085 | Rare:122 |