| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25247832-25248523 | Common:7; Rare:703 | ||||
| chr20:25309783-25310240 | Common:3; Rare:156 | ||||
| chr20:25310240-25310710 | Rare:217 | ||||
| chr20:25390085-25391151 | Common:42; Rare:1059; Clinvar:22; Clinvar (benign):15 | ||||
| chr20:25407422-25407822 | Common:16; Rare:482; Clinvar (pathogenic):2 | ||||
| chr20:25623610-25624670 | Common:13; Rare:982 | ||||
| chr20:25696015-25696415 | Common:6; Rare:100 | ||||
| chr20:25696509-25696660 | Common:2; Rare:109 | ||||
| chr20:25696650-25697150 | Common:18; Rare:652 | ||||
| chr20:25861596-25861812 | Common:5; Rare:117 | ||||
| chr20:25863172-25863572 | Common:5; Rare:208 | ||||
| chr20:31514210-31514552 | Common:18; Rare:309 | ||||
| chr20:31546884-31547479 | Common:1; Rare:448 | ||||
| chr20:31548228-31548628 | Common:2; Rare:77 | ||||
| chr20:31605005-31605405 | Common:44; Rare:655 |