| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:21665912-21666059 | Rare:43 | ||||
| chr22:21952819-21952969 | Common:1; Rare:56 | ||||
| chr22:21982754-21982883 | Rare:35 | ||||
| chr22:22508717-22508892 | Rare:53 | ||||
| chr22:23857641-23857918 | Common:2; Rare:96 | ||||
| chr22:23894574-23894789 | Common:3; Rare:82 | ||||
| chr22:23979725-23979976 | Common:1; Rare:1 | ||||
| chr22:24270651-24270911 | Common:3; Rare:105 | ||||
| chr22:24555901-24556066 | Rare:48 | ||||
| chr22:24952616-24952732 | Rare:35 | ||||
| chr22:26483758-26483874 | Common:4; Rare:49; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512428-26512565 | Common:1; Rare:60 | ||||
| chr22:27801065-27801296 | Common:2; Rare:51 | ||||
| chr22:27801716-27801881 | Common:1; Rare:40 | ||||
| chr22:27919187-27919538 | Common:5; Rare:158 |