| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19854775-19855023 | Common:2; Rare:92 | ||||
| chr22:19941708-19941878 | Rare:74; Clinvar:6; Clinvar (benign):4 | ||||
| chr22:19963110-19963198 | Rare:22 | ||||
| chr22:20016681-20017023 | Common:6; Rare:120 | ||||
| chr22:20020873-20021189 | Common:2; Rare:101 | ||||
| chr22:20079936-20080300 | Common:1; Rare:122 | ||||
| chr22:20116952-20117583 | Common:4; Rare:186 | ||||
| chr22:20319972-20320160 | Common:2; Rare:69 | ||||
| chr22:20394054-20394196 | Rare:34 | ||||
| chr22:20495768-20495994 | Common:2; Rare:83 | ||||
| chr22:20582852-20583148 | Rare:86 | ||||
| chr22:20858969-20859129 | Common:6; Rare:91; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:20917236-20917484 | Rare:93 | ||||
| chr22:20982190-20982363 | Common:2; Rare:44; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:21002053-21002289 | Common:6; Rare:91 |