| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:34105693-34105809 | Rare:21 | ||||
| chr20:34105870-34105911 | Rare:10 | ||||
| chr20:34243496-34243752 | Rare:35 | ||||
| chr20:34292401-34292678 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:34364049-34364402 | Common:1; Rare:88 | ||||
| chr20:34373903-34374102 | Rare:51 | ||||
| chr20:34429473-34429699 | Rare:50 | ||||
| chr20:34447195-34447399 | Rare:32 | ||||
| chr20:34464062-34464289 | Common:1; Rare:55 | ||||
| chr20:34465484-34465570 | Common:2; Rare:23 | ||||
| chr20:34526219-34526288 | Rare:19 | ||||
| chr20:34686788-34686865 | Rare:12 | ||||
| chr20:34707154-34707284 | Common:2; Rare:21 | ||||
| chr20:34707909-34708118 | Rare:34 | ||||
| chr20:34722449-34722682 | Common:1; Rare:39 |