| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44939861-44940060 | Common:3; Rare:54 | ||||
| chr21:45287879-45288085 | Common:5; Rare:80 | ||||
| chr21:45404941-45405194 | Common:12; Rare:153 | ||||
| chr21:45455627-45455965 | Common:6; Rare:142; Clinvar (benign):3 | ||||
| chr21:45456011-45456248 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:45505165-45505430 | Common:4; Rare:157; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr21:45534755-45534879 | Rare:29 | ||||
| chr21:45987017-45987161 | Common:1; Rare:54; Clinvar:8; Clinvar (benign):4 | ||||
| chr21:46286012-46286412 | Common:5; Rare:126 | ||||
| chr21:46320637-46320707 | Common:1; Rare:17 | ||||
| chr21:46323784-46324238 | Common:3; Rare:175; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458686-46459070 | Common:3; Rare:132 | ||||
| chr22:17159175-17159385 | Common:6; Rare:99 | ||||
| chr22:17628699-17628872 | Common:1; Rare:59 | ||||
| chr22:17638668-17638827 | Rare:57 |