| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:101877468-101877804 | Common:5; Rare:86 | ||||
| chr12:102120050-102120269 | Common:1; Rare:88 | ||||
| chr12:103930031-103930571 | Common:9; Rare:178 | ||||
| chr12:103965664-103965941 | Common:2; Rare:73 | ||||
| chr12:104064449-104064555 | Rare:27 | ||||
| chr12:104138147-104138401 | Common:1; Rare:66 | ||||
| chr12:104286765-104287140 | Common:3; Rare:68 | ||||
| chr12:104287203-104287430 | Rare:59 | ||||
| chr12:105107612-105107795 | Common:1; Rare:84 | ||||
| chr12:105236041-105236300 | Common:2; Rare:112 | ||||
| chr12:106955635-106955923 | Rare:104 | ||||
| chr12:106956657-106956853 | Rare:33 | ||||
| chr12:107685638-107685945 | Common:2; Rare:95 | ||||
| chr12:108561145-108561403 | Common:2; Rare:63 | ||||
| chr12:108562394-108562664 | Common:8; Rare:114; Clinvar:2; Clinvar (benign):3 |