| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:41618339-41618803 | Common:3; Rare:135 | ||||
| chr20:43457802-43457913 | Rare:51 | ||||
| chr20:43458238-43458507 | Common:3; Rare:100 | ||||
| chr20:43590650-43591087 | Rare:106 | ||||
| chr20:43666914-43667301 | Common:3; Rare:133 | ||||
| chr20:44187017-44187252 | Common:4; Rare:63 | ||||
| chr20:44210620-44211106 | Common:5; Rare:170 | ||||
| chr20:44475783-44475945 | Rare:68 | ||||
| chr20:44531752-44531969 | Common:1; Rare:72 | ||||
| chr20:44651616-44651822 | Common:1; Rare:66; Clinvar (benign):1 | ||||
| chr20:44885404-44885884 | Common:7; Rare:143 | ||||
| chr20:44938002-44938090 | Rare:31 | ||||
| chr20:44960209-44960514 | Common:1; Rare:118 | ||||
| chr20:44966252-44966571 | Common:2; Rare:117 | ||||
| chr20:45348382-45348477 | Common:1; Rare:28 |