| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36319983-36320258 | Common:4; Rare:134 | ||||
| chr21:37073015-37073374 | Common:5; Rare:139 | ||||
| chr21:37267309-37267617 | Common:3; Rare:104 | ||||
| chr21:39313487-39313617 | Common:2; Rare:77 | ||||
| chr21:39380250-39380511 | Common:1; Rare:124 | ||||
| chr21:39445769-39445883 | Common:2; Rare:35 | ||||
| chr21:41508152-41508310 | Common:1; Rare:30 | ||||
| chr21:42496200-42496536 | Common:2; Rare:82 | ||||
| chr21:42514433-42514498 | Rare:12 | ||||
| chr21:42653450-42653812 | Common:5; Rare:55 | ||||
| chr21:42879525-42879665 | Common:3; Rare:47 | ||||
| chr21:42893050-42893342 | Common:4; Rare:97 | ||||
| chr21:42974242-42974621 | Common:1; Rare:146 | ||||
| chr21:43776260-43776599 | Common:4; Rare:117; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr21:43789355-43789640 | Common:1; Rare:106 |