| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:98515428-98515882 | Rare:165; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:98645018-98645296 | Common:2; Rare:80 | ||||
| chr12:100142833-100143023 | Common:3; Rare:72 | ||||
| chr12:100200707-100200868 | Rare:53 | ||||
| chr12:100267047-100267326 | Common:1; Rare:120 | ||||
| chr12:100573557-100573761 | Rare:71 | ||||
| chr12:101209894-101209962 | Common:1; Rare:20 | ||||
| chr12:101407641-101408061 | Common:3; Rare:107 | ||||
| chr12:102120048-102120257 | Rare:84 | ||||
| chr12:103929959-103930563 | Common:9; Rare:197 | ||||
| chr12:103957107-103957329 | Common:6; Rare:63 | ||||
| chr12:103965664-103965977 | Common:2; Rare:76 | ||||
| chr12:104064372-104064586 | Common:1; Rare:53 | ||||
| chr12:104138147-104138360 | Rare:47 | ||||
| chr12:105107609-105107795 | Common:1; Rare:85 |