| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:94459833-94460057 | Common:2; Rare:68 | ||||
| chr12:98515431-98515653 | Rare:75; Clinvar:1 | ||||
| chr12:98644986-98645290 | Common:2; Rare:90 | ||||
| chr12:100200657-100200846 | Common:1; Rare:59 | ||||
| chr12:101407738-101408076 | Common:2; Rare:85 | ||||
| chr12:102120065-102120251 | Rare:71 | ||||
| chr12:103965705-103965910 | Common:2; Rare:53 | ||||
| chr12:104138170-104138408 | Common:1; Rare:66 | ||||
| chr12:105107612-105107785 | Common:1; Rare:78 | ||||
| chr12:105236090-105236259 | Common:1; Rare:80 | ||||
| chr12:107685685-107685852 | Rare:54 | ||||
| chr12:108562394-108562651 | Common:6; Rare:103; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:109093618-109093903 | Common:2; Rare:64 | ||||
| chr12:109097847-109098204 | Common:4; Rare:113 | ||||
| chr12:109477287-109477638 | Common:3; Rare:85 |