| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19178607-19178932 | Common:2; Rare:115; Clinvar (benign):3 | ||||
| chr22:19291648-19291988 | Common:12; Rare:127 | ||||
| chr22:19432412-19432606 | Common:2; Rare:82 | ||||
| chr22:19447677-19447946 | Common:2; Rare:112 | ||||
| chr22:19467984-19468056 | Rare:14 | ||||
| chr22:19479086-19479509 | Common:4; Rare:149 | ||||
| chr22:19479687-19479981 | Common:4; Rare:83 | ||||
| chr22:19719090-19719153 | Rare:24 | ||||
| chr22:19854795-19855033 | Rare:91 | ||||
| chr22:19941715-19941889 | Rare:75; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:19950887-19951019 | Rare:32 | ||||
| chr22:20020899-20021141 | Common:1; Rare:79 | ||||
| chr22:20080035-20080293 | Rare:91 | ||||
| chr22:20105923-20106195 | Common:1; Rare:61 | ||||
| chr22:20115802-20115955 | Common:1; Rare:43 |