| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109093626-109093903 | Common:2; Rare:62 | ||||
| chr12:109097961-109098418 | Common:5; Rare:153 | ||||
| chr12:109154557-109154686 | Common:1; Rare:34 | ||||
| chr12:109477260-109477685 | Common:3; Rare:116 | ||||
| chr12:109573430-109573863 | Common:3; Rare:140; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr12:109880271-109880676 | Common:1; Rare:129 | ||||
| chr12:109900189-109900356 | Rare:64 | ||||
| chr12:109999103-109999224 | Rare:19 | ||||
| chr12:110281015-110281193 | Rare:71 | ||||
| chr12:110345323-110345681 | Common:1; Rare:71 | ||||
| chr12:110450242-110450388 | Common:2; Rare:57 | ||||
| chr12:110468725-110468902 | Rare:51 | ||||
| chr12:110501477-110501622 | Common:1; Rare:44 | ||||
| chr12:110502047-110502210 | Common:1; Rare:60 | ||||
| chr12:110742643-110742687 | Common:1; Rare:9 |