| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:64063201-64063265 | Rare:24 | ||||
| chr20:64079924-64080116 | Common:2; Rare:80 | ||||
| chr20:64255564-64255796 | Common:3; Rare:110 | ||||
| chr21:15064994-15065169 | Rare:60 | ||||
| chr21:17612841-17613043 | Rare:88 | ||||
| chr21:17819321-17819374 | Rare:23 | ||||
| chr21:25734853-25734983 | Common:2; Rare:59 | ||||
| chr21:25734991-25735443 | Common:1; Rare:142 | ||||
| chr21:25735637-25735854 | Common:3; Rare:49 | ||||
| chr21:28992819-28993110 | Common:2; Rare:123 | ||||
| chr21:29019297-29019389 | Common:5; Rare:44 | ||||
| chr21:29024520-29024726 | Common:2; Rare:86 | ||||
| chr21:29073511-29073885 | Common:2; Rare:120 | ||||
| chr21:29298631-29298947 | Common:3; Rare:127 | ||||
| chr21:31659515-31659837 | Common:2; Rare:140; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 |