| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45833752-45833851 | Common:3; Rare:21 | ||||
| chr20:45834037-45834228 | Rare:71 | ||||
| chr20:45857299-45857621 | Common:4; Rare:89 | ||||
| chr20:45881053-45881260 | Common:2; Rare:51 | ||||
| chr20:45887556-45887736 | Common:2; Rare:50 | ||||
| chr20:45891206-45891413 | Common:1; Rare:64; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45897429-45897798 | Common:2; Rare:67; Clinvar (pathogenic):1 | ||||
| chr20:45912140-45912325 | Common:3; Rare:39 | ||||
| chr20:45934536-45934731 | Common:1; Rare:93 | ||||
| chr20:45935045-45935365 | Rare:127 | ||||
| chr20:45971828-45972036 | Common:1; Rare:60 | ||||
| chr20:45972172-45972564 | Common:1; Rare:138 | ||||
| chr20:46021626-46021720 | Common:2; Rare:28 | ||||
| chr20:46089863-46090130 | Common:1; Rare:89 | ||||
| chr20:46118179-46118344 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):3 |