| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43728526-43728643 | Rare:29 | ||||
| chr21:43728690-43728959 | Common:2; Rare:78 | ||||
| chr21:43776257-43776665 | Common:4; Rare:141; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr21:43789098-43789156 | Rare:15 | ||||
| chr21:43789336-43789690 | Common:2; Rare:129 | ||||
| chr21:43789957-43789982 | Common:1; Rare:2 | ||||
| chr21:43865221-43865396 | Rare:58 | ||||
| chr21:43866281-43866490 | Common:1; Rare:44 | ||||
| chr21:43866520-43866670 | Rare:41 | ||||
| chr21:43866764-43867001 | Common:1; Rare:49 | ||||
| chr21:44012096-44012387 | Common:2; Rare:102 | ||||
| chr21:44012503-44013152 | Rare:207 | ||||
| chr21:44089304-44089504 | Rare:46 | ||||
| chr21:44299509-44299784 | Common:1; Rare:80 | ||||
| chr21:44299859-44300132 | Common:2; Rare:100; Clinvar (benign):1 |