| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:461961-462085 | Rare:24 | ||||
| chr20:462416-462701 | Common:3; Rare:128; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:543616-543879 | Rare:93 | ||||
| chr20:653175-653279 | Common:3; Rare:51 | ||||
| chr20:653441-653600 | Common:1; Rare:45 | ||||
| chr20:833408-833837 | Common:5; Rare:116 | ||||
| chr20:833886-833954 | Rare:22 | ||||
| chr20:1118315-1118730 | Common:7; Rare:119 | ||||
| chr20:1266137-1266350 | Common:3; Rare:44 | ||||
| chr20:1325135-1325499 | Common:1; Rare:85 | ||||
| chr20:1325716-1325947 | Common:2; Rare:46 | ||||
| chr20:1392590-1392645 | Common:1; Rare:11 | ||||
| chr20:1392967-1393288 | Common:2; Rare:129 | ||||
| chr20:1466196-1466483 | Rare:86 | ||||
| chr20:1466771-1466880 | Rare:44 |