| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35455665-35455877 | Rare:33 | ||||
| chr20:35541776-35542182 | Common:5; Rare:227 | ||||
| chr20:35542220-35542620 | Rare:232 | ||||
| chr20:35556757-35557176 | Common:4; Rare:203 | ||||
| chr20:35615771-35615894 | Rare:22 | ||||
| chr20:35616123-35616680 | Common:10; Rare:368 | ||||
| chr20:35616739-35617190 | Common:5; Rare:163 | ||||
| chr20:35619270-35619560 | Rare:205 | ||||
| chr20:35664285-35664540 | Common:2; Rare:57 | ||||
| chr20:35664782-35665135 | Common:4; Rare:226 | ||||
| chr20:35699217-35699703 | Rare:310; Clinvar (benign):9 | ||||
| chr20:35740748-35741248 | Common:6; Rare:211 | ||||
| chr20:35741591-35741751 | Common:3; Rare:79 | ||||
| chr20:35741928-35742722 | Common:18; Rare:562 | ||||
| chr20:35771766-35772116 | Common:5; Rare:197 |