| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:28741787-28742052 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):4 | ||||
| chr22:28800508-28800687 | Common:4; Rare:79 | ||||
| chr22:29268015-29268344 | Common:2; Rare:104 | ||||
| chr22:29767053-29767401 | Common:4; Rare:109 | ||||
| chr22:30356868-30356983 | Common:1; Rare:38 | ||||
| chr22:30607061-30607248 | Common:3; Rare:57; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:30635496-30635783 | Common:8; Rare:87 | ||||
| chr22:37019439-37019836 | Common:5; Rare:110 | ||||
| chr22:37849300-37849465 | Rare:99 | ||||
| chr22:37953555-37953737 | Rare:72 | ||||
| chr22:38656602-38656744 | Rare:39 | ||||
| chr22:38681813-38682010 | Common:2; Rare:84 | ||||
| chr22:39319601-39319764 | Common:3; Rare:75 | ||||
| chr22:40346409-40346556 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40856964-40857148 | Rare:79; Clinvar:3 |