| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:2624269-2624488 | Common:1; Rare:49 | ||||
| chr20:3200014-3200459 | Common:2; Rare:130 | ||||
| chr20:3784371-3784662 | Rare:59 | ||||
| chr20:3800237-3800510 | Common:1; Rare:95 | ||||
| chr20:3804290-3804680 | Common:2; Rare:90 | ||||
| chr20:3808168-3808365 | Common:3; Rare:38 | ||||
| chr20:4822516-4822806 | Common:5; Rare:64 | ||||
| chr20:5592715-5592831 | Rare:15 | ||||
| chr20:5602556-5602743 | Rare:43 | ||||
| chr20:5609794-5610024 | Common:3; Rare:42 | ||||
| chr20:5610351-5610373 | Rare:4 | ||||
| chr20:6036685-6036908 | Common:2; Rare:29 | ||||
| chr20:6040099-6040257 | Rare:28 | ||||
| chr20:6769953-6770165 | Rare:57 | ||||
| chr20:6770353-6770606 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 |