| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23767933-23768051 | Rare:31 | ||||
| chr22:23857787-23857916 | Common:2; Rare:41 | ||||
| chr22:23894045-23894582 | Common:5; Rare:169 | ||||
| chr22:24011677-24011757 | Rare:17 | ||||
| chr22:24245058-24245205 | Rare:26 | ||||
| chr22:24555030-24555437 | Common:4; Rare:144 | ||||
| chr22:24555854-24556045 | Rare:63 | ||||
| chr22:25741861-25742287 | Common:2; Rare:89 | ||||
| chr22:26483773-26483959 | Common:4; Rare:75; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512413-26512550 | Common:1; Rare:59 | ||||
| chr22:26590071-26590225 | Common:3; Rare:64 | ||||
| chr22:27919195-27919504 | Common:5; Rare:139 | ||||
| chr22:28741804-28742074 | Common:2; Rare:77; Clinvar:1 | ||||
| chr22:28800308-28800709 | Common:6; Rare:142 | ||||
| chr22:29205806-29206020 | Rare:58 |