| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:36905413-36905571 | Rare:39; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr20:37344476-37344816 | Common:5; Rare:62 | ||||
| chr20:37345044-37345146 | Rare:12 | ||||
| chr20:37345975-37346226 | Rare:61 | ||||
| chr20:37527806-37528196 | Common:5; Rare:139 | ||||
| chr20:38033416-38033556 | Common:1; Rare:44 | ||||
| chr20:38033686-38033775 | Rare:18 | ||||
| chr20:38165226-38165373 | Common:1; Rare:45 | ||||
| chr20:38472600-38472873 | Common:1; Rare:90 | ||||
| chr20:38805603-38805754 | Common:2; Rare:34 | ||||
| chr20:38962097-38962388 | Common:2; Rare:122 | ||||
| chr20:40689232-40689465 | Common:1; Rare:78 | ||||
| chr20:41028534-41028969 | Rare:151 | ||||
| chr20:41136838-41136993 | Rare:65 | ||||
| chr20:41137363-41137664 | Common:1; Rare:102 |