| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44873506-44874088 | Common:9; Rare:216 | ||||
| chr21:44928653-44928657 | |||||
| chr21:44939851-44940060 | Common:4; Rare:56 | ||||
| chr21:45287861-45288108 | Common:6; Rare:97 | ||||
| chr21:45404874-45405205 | Common:13; Rare:186 | ||||
| chr21:45981543-45981946 | Common:24; Rare:107; Clinvar:5; Clinvar (benign):4 | ||||
| chr21:45986627-45987175 | Common:7; Rare:190; Clinvar:27; Clinvar (benign):14 | ||||
| chr21:46184409-46184759 | Common:4; Rare:32 | ||||
| chr21:46286209-46286412 | Common:4; Rare:78 | ||||
| chr21:46286579-46286665 | Common:1; Rare:26 | ||||
| chr21:46323821-46324202 | Common:2; Rare:135; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46324459-46324662 | Common:4; Rare:77 | ||||
| chr21:46458686-46459067 | Common:3; Rare:131 | ||||
| chr21:46635520-46635761 | Common:3; Rare:80 | ||||
| chr22:17158900-17159389 | Common:11; Rare:193 |