| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:38911605-38911778 | Rare:30 | ||||
| chr21:38913086-38913206 | Common:1; Rare:26 | ||||
| chr21:38913438-38913715 | Common:9; Rare:72 | ||||
| chr21:38959190-38959457 | Rare:52 | ||||
| chr21:39082774-39082934 | Common:18; Rare:52 | ||||
| chr21:42008951-42009302 | Common:2; Rare:84 | ||||
| chr21:42038087-42038244 | Common:2; Rare:38 | ||||
| chr21:42615066-42615231 | Common:2; Rare:40 | ||||
| chr21:44316260-44316496 | Common:1; Rare:89 | ||||
| chr21:44482761-44483058 | Common:2; Rare:48 | ||||
| chr21:44912128-44912211 | Rare:21 | ||||
| chr21:45486584-45486915 | Common:7; Rare:80; Clinvar:1 | ||||
| chr21:45509803-45510261 | Common:11; Rare:194; Clinvar:3; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr21:45511965-45512463 | Common:4; Rare:195; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr21:46149580-46149594 | Rare:4 |