| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:27919195-27919437 | Common:4; Rare:110 | ||||
| chr22:28741810-28742079 | Common:2; Rare:80 | ||||
| chr22:28800406-28800689 | Common:5; Rare:108 | ||||
| chr22:29268005-29268334 | Common:2; Rare:103 | ||||
| chr22:29767053-29767409 | Common:4; Rare:111 | ||||
| chr22:30356864-30356985 | Common:1; Rare:40 | ||||
| chr22:30607054-30607258 | Common:3; Rare:64; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:31160111-31160206 | Common:1; Rare:35 | ||||
| chr22:37019423-37019839 | Common:5; Rare:119 | ||||
| chr22:37849300-37849446 | Rare:88 | ||||
| chr22:37953620-37953731 | Rare:46 | ||||
| chr22:39319611-39319734 | Common:2; Rare:59 | ||||
| chr22:40346441-40346578 | Rare:61; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:41286174-41286429 | Common:2; Rare:77 | ||||
| chr22:41469047-41469167 | Rare:54 |