| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49915496-49915596 | Common:3; Rare:31 | ||||
| chr20:50113116-50113241 | Common:5; Rare:61 | ||||
| chr20:50115906-50116087 | Common:2; Rare:48 | ||||
| chr20:50153633-50153928 | Common:2; Rare:118 | ||||
| chr20:50958446-50958884 | Common:1; Rare:170; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:52972665-52972792 | Common:2; Rare:29 | ||||
| chr20:53593793-53593937 | Common:1; Rare:55 | ||||
| chr20:54173982-54174049 | Rare:19 | ||||
| chr20:56392153-56392550 | Common:3; Rare:112 | ||||
| chr20:56468536-56468700 | Rare:74 | ||||
| chr20:56629993-56630270 | Common:3; Rare:75 | ||||
| chr20:57266042-57266433 | Common:1; Rare:91 | ||||
| chr20:57266602-57266775 | Common:1; Rare:50 | ||||
| chr20:58309410-58309715 | Common:2; Rare:121 | ||||
| chr20:58651057-58651305 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):1 |