| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:29024876-29024979 | Rare:19 | ||||
| chr21:29073606-29073850 | Common:2; Rare:69 | ||||
| chr21:31659502-31659787 | Common:2; Rare:131; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr21:32279017-32279214 | Common:3; Rare:84 | ||||
| chr21:32392971-32393171 | Common:2; Rare:84 | ||||
| chr21:32727862-32728129 | Rare:125; Clinvar:2 | ||||
| chr21:32771782-32772176 | Common:13; Rare:169 | ||||
| chr21:33266262-33266458 | Rare:64; Clinvar:3 | ||||
| chr21:33324734-33325068 | Common:4; Rare:124 | ||||
| chr21:33479854-33480147 | Rare:101 | ||||
| chr21:33491713-33491793 | Rare:16 | ||||
| chr21:33542080-33542221 | Rare:55 | ||||
| chr21:33542794-33543095 | Common:3; Rare:109 | ||||
| chr21:33642201-33642612 | Common:2; Rare:153 | ||||
| chr21:36060308-36060613 | Common:5; Rare:84 |