| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:33266255-33266465 | Rare:66; Clinvar:3 | ||||
| chr21:33324813-33325058 | Common:4; Rare:102 | ||||
| chr21:33479854-33480190 | Common:1; Rare:112 | ||||
| chr21:33491683-33491861 | Rare:48 | ||||
| chr21:33542080-33542196 | Rare:41 | ||||
| chr21:33542805-33543169 | Common:3; Rare:122 | ||||
| chr21:33642201-33642545 | Common:1; Rare:134 | ||||
| chr21:36060308-36060583 | Common:3; Rare:70 | ||||
| chr21:37072511-37072784 | Common:7; Rare:132; Clinvar (pathogenic):1 | ||||
| chr21:37072991-37073402 | Common:5; Rare:155 | ||||
| chr21:37267271-37267727 | Common:4; Rare:167 | ||||
| chr21:38256728-38257037 | Common:2; Rare:55 | ||||
| chr21:38272371-38272535 | Common:1; Rare:29 | ||||
| chr21:38498436-38498722 | Common:1; Rare:37 | ||||
| chr21:39183382-39183582 | Common:5; Rare:81 |