| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10558733-10558946 | Common:2; Rare:34 | ||||
| chr20:10591053-10591214 | Common:1; Rare:21 | ||||
| chr20:10592994-10593179 | Rare:36 | ||||
| chr20:10619518-10619766 | Rare:40 | ||||
| chr20:10642474-10642739 | Rare:61; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr20:10643121-10643179 | Rare:8 | ||||
| chr20:10644860-10645229 | Common:1; Rare:95; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr20:10655373-10655395 | Rare:2 | ||||
| chr20:10659838-10660004 | Rare:33 | ||||
| chr20:10660056-10660372 | Common:6; Rare:62 | ||||
| chr20:10663959-10664121 | Common:2; Rare:34; Clinvar:1; Clinvar (benign):6 | ||||
| chr20:10667793-10668086 | Common:1; Rare:63 | ||||
| chr20:11015722-11015896 | Common:2; Rare:33 | ||||
| chr20:11156980-11157406 | Common:5; Rare:83 | ||||
| chr20:11159125-11159236 | Common:1; Rare:28 |