| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19291671-19291893 | Common:10; Rare:74 | ||||
| chr22:19432325-19432599 | Common:3; Rare:118 | ||||
| chr22:19447677-19447938 | Common:2; Rare:109 | ||||
| chr22:19854809-19855054 | Common:1; Rare:93 | ||||
| chr22:19941722-19941889 | Rare:71; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20079936-20080292 | Common:1; Rare:117 | ||||
| chr22:20319999-20320166 | Common:1; Rare:58 | ||||
| chr22:20495781-20495919 | Common:1; Rare:54 | ||||
| chr22:20982196-20982347 | Common:2; Rare:34; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002061-21002224 | Common:3; Rare:63 | ||||
| chr22:23857766-23857916 | Common:2; Rare:48 | ||||
| chr22:23894259-23894543 | Common:3; Rare:106 | ||||
| chr22:24555843-24556071 | Rare:70 | ||||
| chr22:25741865-25742235 | Common:2; Rare:83 | ||||
| chr22:26483763-26483964 | Common:4; Rare:83; Clinvar:5; Clinvar (benign):1 |