| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:20712571-20712754 | Common:2; Rare:64 | ||||
| chr20:20712802-20713119 | Common:1; Rare:81 | ||||
| chr20:21125784-21126167 | Common:3; Rare:135 | ||||
| chr20:21303127-21303422 | Rare:101 | ||||
| chr20:21303655-21303857 | Rare:60 | ||||
| chr20:23350259-23350992 | Common:6; Rare:217 | ||||
| chr20:23351194-23351485 | Common:1; Rare:83 | ||||
| chr20:23361589-23362250 | Common:8; Rare:222 | ||||
| chr20:23362709-23362824 | Common:1; Rare:23 | ||||
| chr20:23421362-23421696 | Common:5; Rare:134 | ||||
| chr20:23637794-23638170 | Common:7; Rare:102; Clinvar (benign):1 | ||||
| chr20:24992654-24993066 | Common:8; Rare:166 | ||||
| chr20:25057510-25057896 | Common:5; Rare:110 | ||||
| chr20:25058035-25058482 | Common:7; Rare:107 | ||||
| chr20:25058978-25059014 | Rare:9 |