| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44210742-44211102 | Common:5; Rare:125 | ||||
| chr20:44521986-44522213 | Common:2; Rare:73 | ||||
| chr20:44966320-44966586 | Common:2; Rare:106 | ||||
| chr20:45834066-45834173 | Rare:38 | ||||
| chr20:45857357-45857651 | Common:3; Rare:80 | ||||
| chr20:45891213-45891391 | Common:1; Rare:58; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:46364386-46364551 | Rare:63 | ||||
| chr20:47318731-47318903 | Common:1; Rare:50 | ||||
| chr20:47318997-47319114 | Common:1; Rare:31 | ||||
| chr20:47352366-47352632 | Common:1; Rare:44 | ||||
| chr20:47356664-47356802 | Rare:28 | ||||
| chr20:47501548-47501993 | Common:2; Rare:139 | ||||
| chr20:49046173-49046349 | Common:3; Rare:54 | ||||
| chr20:49278035-49278278 | Rare:67 | ||||
| chr20:50113112-50113229 | Common:5; Rare:55 |