| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:53594016-53594151 | Common:2; Rare:33 | ||||
| chr20:54172350-54172970 | Common:4; Rare:120; Clinvar (pathogenic):2 | ||||
| chr20:54172970-54173360 | Common:6; Rare:161; Clinvar:4; Clinvar (benign):1 | ||||
| chr20:54173380-54173736 | Common:8; Rare:187; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr20:54173939-54174134 | Common:2; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:54174152-54174406 | Common:8; Rare:89 | ||||
| chr20:56391710-56392110 | Common:8; Rare:114 | ||||
| chr20:56392125-56392709 | Common:12; Rare:312 | ||||
| chr20:56411830-56412130 | Common:2; Rare:77 | ||||
| chr20:56468417-56468749 | Rare:186 | ||||
| chr20:57391135-57391471 | Common:18; Rare:261 | ||||
| chr20:58309430-58309799 | Common:5; Rare:282 | ||||
| chr20:58388998-58389331 | Common:4; Rare:170; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:58651071-58651373 | Common:4; Rare:137; Clinvar:4; Clinvar (benign):2 | ||||
| chr20:58652160-58652640 | Common:5; Rare:227 |