| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:32762087-32762513 | Common:7; Rare:295; Clinvar:5 | ||||
| chr20:32762478-32762706 | Rare:118; Clinvar:4 | ||||
| chr20:32819708-32820041 | Common:6; Rare:213 | ||||
| chr20:32820086-32820350 | Common:2; Rare:143 | ||||
| chr20:33401421-33401652 | Rare:135 | ||||
| chr20:33443580-33444180 | Common:4; Rare:311; Clinvar:11; Clinvar (benign):6 | ||||
| chr20:33489701-33490645 | Common:10; Rare:556 | ||||
| chr20:33662672-33663490 | Common:2; Rare:232 | ||||
| chr20:33663612-33663902 | Common:3; Rare:152 | ||||
| chr20:33666620-33667074 | Common:1; Rare:298 | ||||
| chr20:33674199-33674625 | Common:2; Rare:203 | ||||
| chr20:33686308-33686693 | Common:5; Rare:185 | ||||
| chr20:33720105-33720592 | Common:16; Rare:376 | ||||
| chr20:33731929-33732476 | Common:5; Rare:308 | ||||
| chr20:33811106-33811482 | Common:1; Rare:116 |