| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46286235-46286396 | Common:4; Rare:60 | ||||
| chr22:17159200-17159357 | Common:4; Rare:72 | ||||
| chr22:19447694-19447836 | Common:1; Rare:52 | ||||
| chr22:19479100-19479471 | Common:4; Rare:137 | ||||
| chr22:19941748-19942124 | Common:2; Rare:98; Clinvar:4 | ||||
| chr22:20117212-20117590 | Common:3; Rare:123 | ||||
| chr22:20495775-20495994 | Common:2; Rare:82 | ||||
| chr22:20858758-20859093 | Common:5; Rare:165; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20982234-20982349 | Common:1; Rare:24; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:24244545-24244663 | Rare:46 | ||||
| chr22:24555030-24555455 | Common:4; Rare:153 | ||||
| chr22:24555617-24556025 | Rare:125 | ||||
| chr22:26483807-26483906 | Common:4; Rare:36; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:26512444-26512565 | Common:1; Rare:54 | ||||
| chr22:27919184-27919504 | Common:5; Rare:142 |