| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:56468341-56468709 | Rare:122 | ||||
| chr20:58692596-58692887 | Common:3; Rare:101 | ||||
| chr20:59032264-59032625 | Common:5; Rare:162; Clinvar (benign):4 | ||||
| chr20:59042729-59043109 | Common:2; Rare:142 | ||||
| chr20:62143307-62143735 | Common:5; Rare:177 | ||||
| chr20:62182959-62183049 | Rare:20 | ||||
| chr20:62386953-62387136 | Common:3; Rare:80 | ||||
| chr20:62937905-62938159 | Common:1; Rare:88 | ||||
| chr20:63707875-63708071 | Rare:55 | ||||
| chr20:63865061-63865322 | Common:2; Rare:90 | ||||
| chr20:63956386-63956531 | Common:1; Rare:59 | ||||
| chr20:63980964-63981161 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr21:25734865-25735006 | Common:2; Rare:69 | ||||
| chr21:25735009-25735239 | Rare:77 | ||||
| chr21:25735591-25735765 | Common:1; Rare:44 |