| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:41322615-41322905 | Common:2; Rare:152 | ||||
| chr21:41420340-41420733 | Common:10; Rare:214 | ||||
| chr21:41506568-41506780 | Common:2; Rare:39 | ||||
| chr21:41506890-41507150 | Rare:88 | ||||
| chr21:41507988-41508422 | Common:10; Rare:215 | ||||
| chr21:41766995-41767218 | Common:9; Rare:169; Clinvar:2; Clinvar (benign):3 | ||||
| chr21:41878966-41879441 | Common:10; Rare:283 | ||||
| chr21:41879450-41879828 | Common:3; Rare:123 | ||||
| chr21:41953911-41954350 | Common:8; Rare:248 | ||||
| chr21:42009861-42010162 | Rare:326 | ||||
| chr21:42010247-42010677 | Common:6; Rare:375 | ||||
| chr21:42218801-42219283 | Common:4; Rare:350 | ||||
| chr21:42220191-42220650 | Common:3; Rare:132 | ||||
| chr21:42313154-42314033 | Common:3; Rare:403 | ||||
| chr21:42315294-42315757 | Common:4; Rare:382 |