| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29299046-29299491 | Common:2; Rare:138 | ||||
| chr21:31659572-31659837 | Common:2; Rare:115; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31731943-31732242 | Common:4; Rare:127 | ||||
| chr21:32279028-32279221 | Common:3; Rare:78 | ||||
| chr21:32392968-32393147 | Common:2; Rare:76 | ||||
| chr21:32727893-32728142 | Rare:120; Clinvar:2 | ||||
| chr21:33266248-33266454 | Rare:63; Clinvar:3 | ||||
| chr21:33324772-33325058 | Common:4; Rare:113 | ||||
| chr21:33479908-33480198 | Common:1; Rare:90 | ||||
| chr21:33542066-33542183 | Rare:43 | ||||
| chr21:33542812-33543161 | Common:3; Rare:117 | ||||
| chr21:33572901-33572932 | Rare:3 | ||||
| chr21:34526753-34527077 | Common:2; Rare:64 | ||||
| chr21:36070233-36070407 | Common:1; Rare:89 | ||||
| chr21:36319980-36320253 | Common:4; Rare:134 |