| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63865040-63865368 | Common:2; Rare:119 | ||||
| chr20:64079924-64080109 | Common:2; Rare:77 | ||||
| chr21:17512846-17513130 | Common:2; Rare:96 | ||||
| chr21:17819324-17819488 | Common:1; Rare:58 | ||||
| chr21:25607458-25607612 | Rare:75 | ||||
| chr21:25734832-25735469 | Common:4; Rare:220 | ||||
| chr21:25735497-25735642 | Rare:33 | ||||
| chr21:25735644-25735765 | Common:1; Rare:28 | ||||
| chr21:26170583-26170926 | Common:5; Rare:109; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:28992800-28993039 | Common:1; Rare:109 | ||||
| chr21:29019307-29019428 | Common:5; Rare:50 | ||||
| chr21:29024537-29024726 | Common:2; Rare:84 | ||||
| chr21:29024876-29025019 | Rare:28 | ||||
| chr21:32279017-32279155 | Common:1; Rare:63 | ||||
| chr21:32392935-32393172 | Common:2; Rare:100 |