| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63956384-63956663 | Common:1; Rare:106 | ||||
| chr20:63980964-63981272 | Common:4; Rare:97; Clinvar:7; Clinvar (benign):4 | ||||
| chr20:64079924-64080115 | Common:2; Rare:79 | ||||
| chr20:64255644-64255771 | Common:3; Rare:64 | ||||
| chr21:5128350-5128586 | Rare:50 | ||||
| chr21:14383120-14383438 | Common:1; Rare:88 | ||||
| chr21:17819324-17819431 | Common:1; Rare:38 | ||||
| chr21:18461095-18461245 | Rare:32 | ||||
| chr21:25607458-25607612 | Rare:75 | ||||
| chr21:25734855-25735440 | Common:3; Rare:206 | ||||
| chr21:25735563-25735912 | Common:4; Rare:94 | ||||
| chr21:28885348-28885413 | Common:2; Rare:51 | ||||
| chr21:28992797-28993130 | Common:2; Rare:138 | ||||
| chr21:29019304-29019414 | Common:5; Rare:47 | ||||
| chr21:29024534-29024722 | Common:2; Rare:83 |