| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:58651113-58651305 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:59042741-59043022 | Common:1; Rare:108 | ||||
| chr20:59940241-59940446 | Rare:81 | ||||
| chr20:62143727-62143792 | Common:1; Rare:28 | ||||
| chr20:62182930-62183049 | Rare:38 | ||||
| chr20:62386938-62387129 | Common:3; Rare:84 | ||||
| chr20:62937858-62938188 | Common:2; Rare:121 | ||||
| chr20:63626961-63627239 | Rare:106 | ||||
| chr20:63658240-63658353 | Common:3; Rare:36 | ||||
| chr20:63707875-63708084 | Rare:61 | ||||
| chr20:63865047-63865351 | Common:2; Rare:111 | ||||
| chr20:63980996-63981224 | Common:4; Rare:75; Clinvar:7; Clinvar (benign):4 | ||||
| chr21:14383173-14383486 | Common:2; Rare:73 | ||||
| chr21:25734853-25735078 | Common:2; Rare:99 | ||||
| chr21:26843067-26843166 | Common:3; Rare:14 |