| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50950584-50950844 | Common:1; Rare:47 | ||||
| chr20:53592510-53592804 | Common:1; Rare:79 | ||||
| chr20:53597660-53597736 | Rare:13 | ||||
| chr20:54156061-54156184 | Common:1; Rare:23 | ||||
| chr20:54158776-54159122 | Common:4; Rare:85; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr20:54162701-54163270 | Common:1; Rare:114; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr20:54165102-54165210 | Common:1; Rare:27 | ||||
| chr20:54165719-54165882 | Rare:49; Clinvar:2 | ||||
| chr20:54166651-54167034 | Common:2; Rare:75 | ||||
| chr20:54167756-54168479 | Common:7; Rare:146 | ||||
| chr20:54168509-54168813 | Common:8; Rare:61 | ||||
| chr20:54168977-54169026 | Rare:15 | ||||
| chr20:54169132-54169817 | Common:6; Rare:160; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:54169825-54170097 | Common:2; Rare:42 | ||||
| chr20:54171313-54171445 | Rare:26 |