| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49278031-49278301 | Rare:73 | ||||
| chr20:49568053-49568152 | Common:1; Rare:23 | ||||
| chr20:49915459-49915822 | Common:4; Rare:112 | ||||
| chr20:49936290-49936437 | Rare:67 | ||||
| chr20:50113106-50113221 | Common:5; Rare:57 | ||||
| chr20:50115883-50116087 | Common:2; Rare:49 | ||||
| chr20:50153635-50153928 | Common:2; Rare:118 | ||||
| chr20:50510089-50510446 | Common:3; Rare:141 | ||||
| chr20:50636881-50637063 | Common:1; Rare:34 | ||||
| chr20:50958454-50958857 | Common:1; Rare:151; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:51801484-51801536 | Common:1; Rare:11 | ||||
| chr20:53593783-53593926 | Common:1; Rare:56 | ||||
| chr20:54475889-54476012 | Common:1; Rare:44 | ||||
| chr20:56392191-56392541 | Common:3; Rare:94 | ||||
| chr20:56392564-56392704 | Common:1; Rare:36 |