| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50115926-50116074 | Common:1; Rare:34 | ||||
| chr20:50153635-50153939 | Common:2; Rare:124 | ||||
| chr20:50510071-50510490 | Common:3; Rare:163 | ||||
| chr20:50958467-50958905 | Common:1; Rare:170; Clinvar:2; Clinvar (benign):4 | ||||
| chr20:51562777-51562993 | Common:3; Rare:42 | ||||
| chr20:52972063-52972502 | Common:3; Rare:109 | ||||
| chr20:52972608-52972646 | Rare:5 | ||||
| chr20:52972653-52973267 | Common:5; Rare:144 | ||||
| chr20:53593797-53593890 | Common:1; Rare:33 | ||||
| chr20:56392191-56392690 | Common:6; Rare:131 | ||||
| chr20:56412016-56412228 | Common:3; Rare:42 | ||||
| chr20:56468402-56468734 | Rare:111 | ||||
| chr20:56629201-56629320 | Rare:40 | ||||
| chr20:57710553-57710649 | Rare:23 | ||||
| chr20:58651133-58651305 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):1 |