| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:26590075-26590250 | Common:3; Rare:70 | ||||
| chr22:27919175-27919536 | Common:5; Rare:161 | ||||
| chr22:28741800-28742082 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:28742214-28742336 | Rare:43 | ||||
| chr22:28742422-28742701 | Common:1; Rare:64 | ||||
| chr22:28800039-28800143 | Common:1; Rare:39 | ||||
| chr22:28800341-28800773 | Common:6; Rare:154 | ||||
| chr22:29267894-29268348 | Common:2; Rare:130 | ||||
| chr22:29581079-29581229 | Common:2; Rare:45 | ||||
| chr22:29767048-29767422 | Common:4; Rare:119 | ||||
| chr22:30289540-30289854 | Common:2; Rare:63 | ||||
| chr22:30326844-30327183 | Common:3; Rare:121 | ||||
| chr22:30356864-30356947 | Rare:29 | ||||
| chr22:30579800-30580108 | Common:2; Rare:89 | ||||
| chr22:30607027-30607334 | Common:3; Rare:102; Clinvar:4; Clinvar (benign):3 |