| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44801739-44801885 | Rare:64 | ||||
| chr21:44873479-44873542 | Rare:21 | ||||
| chr21:44873600-44874088 | Common:9; Rare:188 | ||||
| chr21:44939871-44940039 | Common:2; Rare:47 | ||||
| chr21:45287835-45288102 | Common:6; Rare:106 | ||||
| chr21:45981519-45981785 | Common:23; Rare:53; Clinvar (benign):1 | ||||
| chr21:46184414-46184754 | Common:4; Rare:31 | ||||
| chr21:46286209-46286408 | Common:4; Rare:76 | ||||
| chr21:46286563-46286688 | Common:1; Rare:39 | ||||
| chr21:46323830-46324206 | Common:2; Rare:132; Clinvar:3; Clinvar (benign):1 | ||||
| chr21:46324459-46324640 | Common:3; Rare:69 | ||||
| chr21:46605011-46605243 | Common:2; Rare:51 | ||||
| chr21:46635457-46635739 | Common:6; Rare:97 | ||||
| chr22:11066053-11066310 | |||||
| chr22:17159149-17159385 | Common:7; Rare:110 |