| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31559767-31559959 | Common:1; Rare:40 | ||||
| chr22:31647770-31647854 | Common:1; Rare:11 | ||||
| chr22:32050736-32051104 | Common:2; Rare:70 | ||||
| chr22:33455486-33455753 | Common:1; Rare:58 | ||||
| chr22:33730867-33730990 | Rare:27 | ||||
| chr22:33921009-33921255 | Common:1; Rare:106 | ||||
| chr22:35756051-35756144 | Rare:20 | ||||
| chr22:35761268-35761429 | Rare:45 | ||||
| chr22:35838078-35838273 | Rare:28 | ||||
| chr22:35838295-35838344 | Rare:12 | ||||
| chr22:35852196-35852476 | Common:1; Rare:48 | ||||
| chr22:35894966-35895097 | Common:1; Rare:35 | ||||
| chr22:36279704-36279835 | Common:1; Rare:27 | ||||
| chr22:36280179-36280475 | Common:6; Rare:55 | ||||
| chr22:36291692-36292258 | Common:3; Rare:155; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 |