| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45834066-45834188 | Rare:42 | ||||
| chr20:45857315-45857639 | Common:3; Rare:94 | ||||
| chr20:45881020-45881241 | Common:2; Rare:50 | ||||
| chr20:45890149-45890316 | Common:1; Rare:62 | ||||
| chr20:45891192-45891379 | Common:1; Rare:62; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45912146-45912253 | Common:3; Rare:25 | ||||
| chr20:45934548-45934761 | Common:2; Rare:104 | ||||
| chr20:45935048-45935351 | Rare:119 | ||||
| chr20:45971700-45972073 | Common:4; Rare:102 | ||||
| chr20:45972154-45972212 | Rare:31 | ||||
| chr20:46021602-46021706 | Common:3; Rare:26 | ||||
| chr20:46021867-46022121 | Rare:69 | ||||
| chr20:46089846-46089928 | Rare:29 | ||||
| chr20:46220841-46221087 | Rare:43 | ||||
| chr20:46363962-46364121 | Common:1; Rare:35 |