| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34955699-34955928 | Common:1; Rare:83; Clinvar:3; Clinvar (benign):3 | ||||
| chr20:35092779-35092966 | Common:2; Rare:78 | ||||
| chr20:35147229-35147416 | Common:1; Rare:69 | ||||
| chr20:35171760-35172159 | Common:2; Rare:90 | ||||
| chr20:35284475-35284886 | Common:3; Rare:124 | ||||
| chr20:35411941-35412101 | Rare:60 | ||||
| chr20:35455034-35455341 | Common:1; Rare:100 | ||||
| chr20:35541878-35542182 | Common:2; Rare:112 | ||||
| chr20:35542359-35542573 | Rare:69 | ||||
| chr20:35556030-35556269 | Rare:75 | ||||
| chr20:35616935-35617080 | Common:1; Rare:25 | ||||
| chr20:35631502-35631731 | Common:3; Rare:76 | ||||
| chr20:35664855-35665053 | Common:1; Rare:52 | ||||
| chr20:35699133-35699638 | Rare:140; Clinvar (benign):3 | ||||
| chr20:35705275-35705636 | Common:3; Rare:87 |