| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20319999-20320133 | Common:1; Rare:49 | ||||
| chr22:20495783-20495904 | Common:1; Rare:46 | ||||
| chr22:20858704-20859105 | Common:7; Rare:203; Clinvar:3; Clinvar (benign):4 | ||||
| chr22:20982196-20982322 | Common:2; Rare:26; Clinvar (benign):2 | ||||
| chr22:21002092-21002250 | Common:4; Rare:56 | ||||
| chr22:23767925-23768046 | Rare:33 | ||||
| chr22:23857660-23857945 | Common:3; Rare:101 | ||||
| chr22:24555884-24556068 | Rare:54 | ||||
| chr22:26483775-26484090 | Common:9; Rare:143; Clinvar:5; Clinvar (benign):2 | ||||
| chr22:26512428-26512552 | Common:1; Rare:55 | ||||
| chr22:26590077-26590220 | Common:3; Rare:58 | ||||
| chr22:27919171-27919478 | Common:5; Rare:132 | ||||
| chr22:28741800-28742078 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:28742578-28742696 | Common:1; Rare:27 | ||||
| chr22:28800363-28800705 | Common:5; Rare:123 |