| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:1392976-1393240 | Common:2; Rare:110 | ||||
| chr20:2102054-2102108 | Common:1; Rare:18 | ||||
| chr20:2470728-2471073 | Common:4; Rare:110 | ||||
| chr20:2508872-2509233 | Common:1; Rare:80 | ||||
| chr20:2652434-2652642 | Common:6; Rare:69 | ||||
| chr20:2652976-2653066 | Rare:25 | ||||
| chr20:2664157-2664307 | Common:4; Rare:68 | ||||
| chr20:2840631-2840782 | Common:1; Rare:62 | ||||
| chr20:3045969-3046128 | Rare:54 | ||||
| chr20:3173483-3173699 | Common:1; Rare:81 | ||||
| chr20:3209439-3209542 | Rare:36 | ||||
| chr20:3470880-3470978 | Common:1; Rare:52 | ||||
| chr20:3767702-3768040 | Common:3; Rare:107 | ||||
| chr20:3846724-3846912 | Common:1; Rare:53 | ||||
| chr20:3889160-3889392 | Common:1; Rare:119; Clinvar:5; Clinvar (benign):2 |