| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25751087-25751185 | Rare:17 | ||||
| chr20:25854008-25854241 | Common:4; Rare:75 | ||||
| chr20:29497235-29497392 | |||||
| chr20:30580109-30580248 | Common:1; Rare:26 | ||||
| chr20:32141662-32141787 | Common:2; Rare:36 | ||||
| chr20:36050288-36050526 | Common:1; Rare:70 | ||||
| chr20:36050538-36050737 | Common:1; Rare:79 | ||||
| chr20:38146818-38147063 | Rare:67 | ||||
| chr20:38148058-38148340 | Common:1; Rare:73 | ||||
| chr20:38435282-38435452 | Common:1; Rare:59 | ||||
| chr20:38446536-38446733 | Common:1; Rare:64 | ||||
| chr20:45419363-45419582 | Common:1; Rare:86; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr20:45424261-45424540 | Common:3; Rare:76; Clinvar (pathogenic):1 | ||||
| chr20:46352208-46352494 | Rare:72 | ||||
| chr20:46583622-46583811 | Common:3; Rare:50 |