| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45404950-45405196 | Common:11; Rare:148 | ||||
| chr21:45981524-45981813 | Common:23; Rare:64; Clinvar (benign):2 | ||||
| chr21:46097311-46097630 | Common:3; Rare:62 | ||||
| chr21:46098389-46098833 | Common:5; Rare:114 | ||||
| chr21:46286250-46286408 | Common:4; Rare:58 | ||||
| chr22:17159175-17159373 | Common:6; Rare:90 | ||||
| chr22:17628623-17628853 | Common:2; Rare:77 | ||||
| chr22:18077827-18078022 | Common:4; Rare:64; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19447690-19447771 | Common:1; Rare:34 | ||||
| chr22:19941721-19942126 | Common:2; Rare:114; Clinvar:5; Clinvar (benign):4 | ||||
| chr22:20117212-20117579 | Common:3; Rare:118 | ||||
| chr22:20319989-20320174 | Common:2; Rare:64 | ||||
| chr22:20495778-20495996 | Common:2; Rare:81 | ||||
| chr22:20507515-20507652 | Rare:47 | ||||
| chr22:20858724-20859088 | Common:4; Rare:185; Clinvar:3; Clinvar (benign):2 |