| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63865071-63865375 | Common:2; Rare:119 | ||||
| chr20:63956368-63956656 | Common:1; Rare:110 | ||||
| chr20:63969837-63970095 | Common:3; Rare:89 | ||||
| chr20:63980969-63981230 | Common:4; Rare:89; Clinvar:7; Clinvar (benign):4 | ||||
| chr20:64079888-64080095 | Common:1; Rare:81 | ||||
| chr21:14383111-14383516 | Common:3; Rare:114 | ||||
| chr21:17512840-17513120 | Common:2; Rare:97 | ||||
| chr21:17612779-17613037 | Common:1; Rare:107 | ||||
| chr21:17819311-17819467 | Common:1; Rare:58 | ||||
| chr21:17819626-17819689 | Rare:17 | ||||
| chr21:25734832-25735082 | Common:2; Rare:105 | ||||
| chr21:25735088-25735440 | Common:1; Rare:104 | ||||
| chr21:25735445-25735715 | Common:2; Rare:72 | ||||
| chr21:26170562-26170928 | Common:6; Rare:119; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:26842914-26843214 | Common:5; Rare:55 |