| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:42009860-42010240 | Common:1; Rare:391 | ||||
| chr21:42010260-42010585 | Common:10; Rare:376 | ||||
| chr21:42010580-42010850 | Common:4; Rare:109 | ||||
| chr21:42388991-42389391 | Common:7; Rare:146; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr21:42402830-42403230 | Common:2; Rare:109 | ||||
| chr21:42403610-42404230 | Common:13; Rare:286 | ||||
| chr21:42496213-42496640 | Common:5; Rare:337 | ||||
| chr21:42499301-42499807 | Common:22; Rare:286 | ||||
| chr21:42513517-42513917 | Common:1; Rare:155 | ||||
| chr21:42514190-42514657 | Common:5; Rare:170 | ||||
| chr21:42878740-42879260 | Common:15; Rare:537 | ||||
| chr21:42879240-42879410 | Rare:65 | ||||
| chr21:42879430-42879760 | Common:21; Rare:586 | ||||
| chr21:42892966-42893396 | Common:30; Rare:786 | ||||
| chr21:42893400-42894365 | Common:8; Rare:288 |