| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:30326855-30327174 | Common:2; Rare:112 | ||||
| chr22:30356803-30356994 | Common:1; Rare:68 | ||||
| chr22:30579922-30580108 | Rare:52 | ||||
| chr22:30607038-30607295 | Common:3; Rare:78; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:31081124-31081345 | Common:1; Rare:57 | ||||
| chr22:31107450-31107710 | Common:2; Rare:86 | ||||
| chr22:31290717-31290906 | Rare:77 | ||||
| chr22:31292401-31292603 | Common:1; Rare:41 | ||||
| chr22:31399452-31399669 | Rare:64 | ||||
| chr22:31489768-31490164 | Common:3; Rare:159 | ||||
| chr22:31496409-31496612 | Common:2; Rare:59 | ||||
| chr22:31749810-31750004 | Common:2; Rare:57 | ||||
| chr22:31753805-31754128 | Common:1; Rare:114 | ||||
| chr22:31944328-31944762 | Common:5; Rare:172 | ||||
| chr22:32042977-32043154 | Common:2; Rare:49; Clinvar (benign):1 |