| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:33922899-33922934 | Rare:10 | ||||
| chr22:35257402-35257546 | Common:1; Rare:47 | ||||
| chr22:35300114-35300296 | Rare:51 | ||||
| chr22:35380642-35381166 | Common:12; Rare:163 | ||||
| chr22:35399894-35400233 | Rare:121 | ||||
| chr22:35840236-35840541 | Common:1; Rare:64 | ||||
| chr22:35961575-35961752 | Common:1; Rare:29 | ||||
| chr22:36239510-36239683 | Rare:54 | ||||
| chr22:36285668-36285882 | Rare:77; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:36329416-36329790 | Common:1; Rare:84 | ||||
| chr22:36387813-36387914 | Rare:18 | ||||
| chr22:36481322-36481404 | Common:1; Rare:18 | ||||
| chr22:36481559-36481688 | Common:2; Rare:39 | ||||
| chr22:36507010-36507249 | Common:4; Rare:89 | ||||
| chr22:36529071-36529562 | Common:8; Rare:155 |