| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43776523-43776657 | Rare:46 | ||||
| chr21:43789377-43789630 | Common:1; Rare:93 | ||||
| chr21:44339226-44339469 | Common:2; Rare:74 | ||||
| chr21:44801709-44801876 | Rare:66 | ||||
| chr21:44873507-44873595 | Rare:23 | ||||
| chr21:44873626-44874080 | Common:9; Rare:175 | ||||
| chr21:44939935-44940049 | Common:1; Rare:36 | ||||
| chr21:45287879-45288085 | Common:5; Rare:80 | ||||
| chr21:45981519-45981897 | Common:24; Rare:96; Clinvar:3; Clinvar (benign):3 | ||||
| chr21:46184411-46184783 | Common:4; Rare:37 | ||||
| chr21:46286222-46286396 | Common:4; Rare:66 | ||||
| chr21:46323806-46324224 | Common:3; Rare:159; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458666-46459108 | Common:4; Rare:151 | ||||
| chr22:17158656-17158729 | Common:2; Rare:13 | ||||
| chr22:17159175-17159395 | Common:6; Rare:110 |