| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45287879-45288093 | Common:5; Rare:82 | ||||
| chr21:45404874-45405188 | Common:12; Rare:180 | ||||
| chr21:45981516-45981814 | Common:23; Rare:66; Clinvar (benign):2 | ||||
| chr21:46286233-46286412 | Common:4; Rare:68 | ||||
| chr21:46323813-46324161 | Common:2; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:17159194-17159385 | Common:5; Rare:91 | ||||
| chr22:17628615-17628852 | Common:2; Rare:78 | ||||
| chr22:19178425-19178519 | Common:1; Rare:26 | ||||
| chr22:19447690-19447775 | Common:1; Rare:36 | ||||
| chr22:19941708-19942124 | Common:2; Rare:121; Clinvar:6; Clinvar (benign):4 | ||||
| chr22:20117124-20117580 | Common:3; Rare:146 | ||||
| chr22:20319982-20320158 | Common:2; Rare:62 | ||||
| chr22:20495772-20495994 | Common:2; Rare:82 | ||||
| chr22:20507458-20507652 | Rare:64 | ||||
| chr22:20858797-20859121 | Common:6; Rare:157; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 |