| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:33324862-33325073 | Common:4; Rare:89 | ||||
| chr21:33403290-33403563 | Common:1; Rare:66 | ||||
| chr21:33479820-33480172 | Common:1; Rare:114 | ||||
| chr21:33542073-33542263 | Rare:74 | ||||
| chr21:33542814-33543169 | Common:2; Rare:117 | ||||
| chr21:34526780-34527072 | Common:1; Rare:53 | ||||
| chr21:36060503-36060584 | Common:1; Rare:23 | ||||
| chr21:36069927-36070081 | Common:8; Rare:49 | ||||
| chr21:36134870-36135087 | Common:1; Rare:48 | ||||
| chr21:36319950-36320267 | Common:4; Rare:149 | ||||
| chr21:36966368-36966502 | Rare:37 | ||||
| chr21:37072490-37072746 | Common:5; Rare:129; Clinvar (pathogenic):1 | ||||
| chr21:37072991-37073402 | Common:5; Rare:155 | ||||
| chr21:37267304-37267695 | Common:4; Rare:141 | ||||
| chr21:37267876-37267987 | Rare:36 |