| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36385218-36385528 | Common:1; Rare:187 | ||||
| chr21:36698876-36699264 | Common:8; Rare:262 | ||||
| chr21:36965610-36966160 | Common:17; Rare:157 | ||||
| chr21:36966260-36966980 | Common:17; Rare:440 | ||||
| chr21:36989730-36990137 | Common:20; Rare:274 | ||||
| chr21:36990147-36990378 | Common:11; Rare:123; Clinvar:1; Clinvar (benign):10 | ||||
| chr21:37006664-37006844 | Common:2; Rare:45 | ||||
| chr21:37006996-37007480 | Common:6; Rare:139 | ||||
| chr21:37071720-37072060 | Common:2; Rare:74 | ||||
| chr21:37072245-37072796 | Common:17; Rare:418; Clinvar (pathogenic):2 | ||||
| chr21:37072979-37073519 | Common:17; Rare:471 | ||||
| chr21:37267257-37267890 | Common:11; Rare:502 | ||||
| chr21:37267810-37268300 | Common:8; Rare:284 | ||||
| chr21:37365750-37366133 | Common:4; Rare:259 | ||||
| chr21:37366056-37366480 | Common:9; Rare:360 |