| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43789349-43789657 | Common:2; Rare:213 | ||||
| chr21:43865006-43865317 | Common:1; Rare:113 | ||||
| chr21:43866510-43867430 | Common:2; Rare:247 | ||||
| chr21:44012145-44012380 | Common:3; Rare:141 | ||||
| chr21:44012620-44012930 | Rare:102 | ||||
| chr21:44299927-44300136 | Common:1; Rare:128; Clinvar (benign):2 | ||||
| chr21:44339205-44339489 | Common:5; Rare:155 | ||||
| chr21:44801740-44801912 | Rare:139 | ||||
| chr21:44817960-44818350 | Common:1; Rare:234 | ||||
| chr21:44873407-44873507 | Common:1; Rare:34 | ||||
| chr21:44873605-44873882 | Common:4; Rare:119 | ||||
| chr21:44914229-44914346 | Common:2; Rare:34 | ||||
| chr21:44920860-44921280 | Common:2; Rare:165; Clinvar:2; Clinvar (benign):2 | ||||
| chr21:44939869-44940090 | Common:4; Rare:123 | ||||
| chr21:45074431-45074650 | Common:6; Rare:244 |