| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50730898-50731559 | Common:9; Rare:733 | ||||
| chr20:50731512-50731637 | Rare:36 | ||||
| chr20:50731579-50732553 | Common:7; Rare:540 | ||||
| chr20:50794714-50795114 | Common:4; Rare:192 | ||||
| chr20:50929083-50930024 | Common:1; Rare:327 | ||||
| chr20:50930000-50930776 | Common:14; Rare:506 | ||||
| chr20:50931141-50931898 | Common:14; Rare:849 | ||||
| chr20:50958404-50958923 | Common:7; Rare:1056; Clinvar:13; Clinvar (benign):24 | ||||
| chr20:51022992-51023392 | Common:1; Rare:241 | ||||
| chr20:51542582-51542982 | Common:18; Rare:275 | ||||
| chr20:52190651-52191444 | Common:5; Rare:131 | ||||
| chr20:52191467-52191854 | Rare:311 | ||||
| chr20:52191920-52192100 | Common:2; Rare:35 | ||||
| chr20:52192260-52192850 | Common:24; Rare:196 | ||||
| chr20:52204129-52204529 | Common:7; Rare:129 |