| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:33642203-33642665 | Common:2; Rare:164 | ||||
| chr21:33642669-33642705 | Rare:13 | ||||
| chr21:34072912-34073236 | Common:4; Rare:94 | ||||
| chr21:36060256-36060613 | Common:5; Rare:97 | ||||
| chr21:36320016-36320258 | Common:3; Rare:118 | ||||
| chr21:36990181-36990437 | Common:5; Rare:83; Clinvar (benign):4 | ||||
| chr21:37072512-37072791 | Common:7; Rare:135; Clinvar (pathogenic):1 | ||||
| chr21:37072983-37073395 | Common:6; Rare:155 | ||||
| chr21:37267296-37267666 | Common:4; Rare:131 | ||||
| chr21:37267685-37267736 | Rare:18 | ||||
| chr21:38498448-38498557 | Rare:13 | ||||
| chr21:39380238-39380516 | Common:1; Rare:128 | ||||
| chr21:39445751-39445919 | Common:3; Rare:55 | ||||
| chr21:39867321-39867636 | Common:1; Rare:81 | ||||
| chr21:41426139-41426270 | Common:1; Rare:27 |