| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50958497-50958866 | Common:1; Rare:129; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:51562835-51563023 | Common:1; Rare:31 | ||||
| chr20:52972045-52972506 | Common:3; Rare:113 | ||||
| chr20:52972667-52972841 | Common:2; Rare:40 | ||||
| chr20:52972877-52973038 | Common:2; Rare:30 | ||||
| chr20:53593783-53593882 | Common:1; Rare:34 | ||||
| chr20:56392213-56392397 | Rare:47 | ||||
| chr20:56629145-56629320 | Rare:53 | ||||
| chr20:58388989-58389271 | Common:3; Rare:124; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:58651053-58651305 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58888792-58888841 | Rare:18 | ||||
| chr20:58981156-58981312 | Common:2; Rare:80 | ||||
| chr20:59042734-59042956 | Common:1; Rare:79 | ||||
| chr20:59933586-59933792 | Common:4; Rare:82 | ||||
| chr20:59940241-59940481 | Rare:96 |