| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20319888-20320151 | Common:2; Rare:99 | ||||
| chr22:20495781-20495999 | Common:2; Rare:82 | ||||
| chr22:20507456-20507723 | Rare:96 | ||||
| chr22:20858780-20859111 | Common:6; Rare:164; Clinvar:3; Clinvar (benign):5 | ||||
| chr22:20917284-20917495 | Rare:79 | ||||
| chr22:20982201-20982361 | Common:2; Rare:37; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002052-21002227 | Common:3; Rare:70 | ||||
| chr22:21642051-21642364 | Common:2; Rare:94 | ||||
| chr22:21867325-21867808 | Common:4; Rare:132 | ||||
| chr22:22520253-22520455 | Common:4; Rare:42 | ||||
| chr22:22558970-22559374 | Common:2; Rare:130 | ||||
| chr22:23145413-23145510 | Rare:41 | ||||
| chr22:23751129-23751189 | Rare:16 | ||||
| chr22:23767907-23768037 | Rare:37 | ||||
| chr22:23787121-23787257 | Rare:41; Clinvar:3; Clinvar (benign):6 |