| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39380244-39380516 | Common:1; Rare:128 | ||||
| chr21:39387632-39387813 | Common:2; Rare:77 | ||||
| chr21:39445729-39445925 | Common:3; Rare:64 | ||||
| chr21:39451644-39452145 | Common:3; Rare:143 | ||||
| chr21:39452602-39452728 | Common:1; Rare:13 | ||||
| chr21:42653473-42653807 | Common:5; Rare:53 | ||||
| chr21:42879025-42879134 | Common:1; Rare:33 | ||||
| chr21:42879520-42879676 | Common:3; Rare:53 | ||||
| chr21:42893042-42893347 | Common:4; Rare:104 | ||||
| chr21:43659443-43659592 | Common:1; Rare:51 | ||||
| chr21:43728592-43728900 | Common:3; Rare:81 | ||||
| chr21:43776207-43776516 | Common:5; Rare:108; Clinvar:5; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr21:43789369-43789638 | Common:1; Rare:100 | ||||
| chr21:44299996-44300117 | Rare:49; Clinvar (benign):1 | ||||
| chr21:44339216-44339506 | Common:3; Rare:83 |