| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:10508943-10509126 | Rare:27 | ||||
| chr20:10511328-10511371 | Rare:5 | ||||
| chr20:10511557-10511704 | Common:1; Rare:20 | ||||
| chr20:10521186-10521354 | Rare:30 | ||||
| chr20:10521442-10521691 | Rare:22 | ||||
| chr20:10539860-10539941 | Rare:11 | ||||
| chr20:10540280-10540444 | Common:2; Rare:17 | ||||
| chr20:10540654-10541009 | Rare:54 | ||||
| chr20:10619561-10619736 | Rare:29 | ||||
| chr20:10667202-10667287 | Common:1; Rare:29 | ||||
| chr20:10671432-10671627 | Common:1; Rare:33 | ||||
| chr20:10672696-10672901 | Common:3; Rare:61; Clinvar:4; Clinvar (benign):3 | ||||
| chr20:10674849-10674973 | Common:1; Rare:27 | ||||
| chr20:11001776-11002048 | Common:2; Rare:59 | ||||
| chr20:11379572-11379834 | Rare:63 |