| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42737189-42737423 | Common:1; Rare:37 | ||||
| chr21:42738154-42738404 | Common:4; Rare:46 | ||||
| chr21:42739169-42739330 | Common:1; Rare:37 | ||||
| chr21:42743529-42743802 | Common:3; Rare:71 | ||||
| chr21:42755813-42756145 | Common:1; Rare:62 | ||||
| chr21:42760528-42760884 | Common:6; Rare:104 | ||||
| chr21:42761021-42761246 | Common:1; Rare:45 | ||||
| chr21:42763192-42763309 | Rare:19 | ||||
| chr21:42844803-42844852 | Rare:5 | ||||
| chr21:44063297-44063626 | Common:2; Rare:68 | ||||
| chr21:45509897-45510259 | Common:5; Rare:155; Clinvar:3; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr21:45530554-45530856 | Common:2; Rare:87 | ||||
| chr21:46437932-46438229 | Rare:73; Clinvar:3 | ||||
| chr22:19177347-19177535 | Common:2; Rare:45 | ||||
| chr22:20954336-20954517 | Rare:37 |