| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:33571303-33571329 | Rare:4 | ||||
| chr21:33642669-33642705 | Rare:13 | ||||
| chr21:33907340-33907720 | Rare:87 | ||||
| chr21:34073166-34073232 | Common:1; Rare:11 | ||||
| chr21:34363568-34363877 | Common:1; Rare:56 | ||||
| chr21:34363882-34364164 | Common:1; Rare:45; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:34526750-34527103 | Common:2; Rare:67 | ||||
| chr21:34668756-34669155 | Common:2; Rare:88 | ||||
| chr21:34669244-34669595 | Common:4; Rare:91 | ||||
| chr21:34887998-34888208 | Common:1; Rare:45 | ||||
| chr21:34888211-34888311 | Rare:19 | ||||
| chr21:34888331-34888690 | Common:1; Rare:90 | ||||
| chr21:36060308-36060604 | Common:3; Rare:77 | ||||
| chr21:36069868-36070403 | Common:9; Rare:224 | ||||
| chr21:36134777-36135087 | Common:2; Rare:60 |