| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45857892-45858120 | Common:1; Rare:75 | ||||
| chr20:45881000-45881296 | Common:2; Rare:66 | ||||
| chr20:45890950-45891435 | Common:4; Rare:146; Clinvar:8; Clinvar (benign):4 | ||||
| chr20:45910894-45911243 | Common:4; Rare:108 | ||||
| chr20:45912140-45912273 | Common:3; Rare:32 | ||||
| chr20:45934589-45934841 | Common:1; Rare:110 | ||||
| chr20:45934870-45935431 | Common:3; Rare:230 | ||||
| chr20:45971818-45972650 | Common:5; Rare:278 | ||||
| chr20:46008773-46008931 | Common:2; Rare:42; Clinvar (pathogenic):1 | ||||
| chr20:46089545-46089768 | Common:3; Rare:86 | ||||
| chr20:46089903-46090053 | Rare:52 | ||||
| chr20:46118022-46118406 | Common:4; Rare:112; Clinvar:2; Clinvar (benign):3 | ||||
| chr20:46118581-46118848 | Common:1; Rare:52 | ||||
| chr20:46363481-46363678 | Rare:26 | ||||
| chr20:46363962-46364161 | Common:1; Rare:39 |