| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:32612483-32612895 | Rare:107 | ||||
| chr21:32727889-32728129 | Rare:118; Clinvar:2 | ||||
| chr21:32771709-32772176 | Common:13; Rare:206 | ||||
| chr21:33266262-33266434 | Rare:56; Clinvar:3 | ||||
| chr21:33324866-33325073 | Common:4; Rare:87 | ||||
| chr21:33403289-33403611 | Common:1; Rare:87; Clinvar:3 | ||||
| chr21:33479854-33480154 | Rare:103 | ||||
| chr21:33542080-33542248 | Rare:67 | ||||
| chr21:33542812-33543188 | Common:3; Rare:123 | ||||
| chr21:33642201-33642665 | Common:2; Rare:164 | ||||
| chr21:33642674-33642711 | Rare:14 | ||||
| chr21:34073143-34073232 | Common:1; Rare:19 | ||||
| chr21:36060345-36060604 | Common:3; Rare:66 | ||||
| chr21:36320016-36320267 | Common:3; Rare:120 | ||||
| chr21:37072491-37072687 | Common:4; Rare:99; Clinvar (pathogenic):1 |