| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:45812351-45812729 | Common:3; Rare:111 | ||||
| chr20:45857314-45857639 | Common:3; Rare:94 | ||||
| chr20:45891256-45891379 | Common:1; Rare:44; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45910945-45911180 | Common:4; Rare:73 | ||||
| chr20:45912150-45912236 | Common:3; Rare:20 | ||||
| chr20:45934548-45934719 | Common:1; Rare:83 | ||||
| chr20:46364377-46364518 | Rare:52 | ||||
| chr20:46406558-46406782 | Common:2; Rare:58 | ||||
| chr20:46513517-46513634 | Common:1; Rare:45 | ||||
| chr20:47318712-47319010 | Common:1; Rare:94 | ||||
| chr20:47351714-47351776 | Rare:11 | ||||
| chr20:47356656-47356887 | Rare:54 | ||||
| chr20:47501698-47502000 | Common:1; Rare:105 | ||||
| chr20:49046115-49046363 | Common:3; Rare:75 | ||||
| chr20:49219281-49219505 | Rare:108 |