| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63865066-63865367 | Common:2; Rare:115 | ||||
| chr20:63951164-63951192 | Rare:4 | ||||
| chr20:64079932-64080082 | Common:1; Rare:63 | ||||
| chr21:14383120-14383481 | Common:2; Rare:99 | ||||
| chr21:17819305-17819420 | Common:1; Rare:45 | ||||
| chr21:25607458-25607584 | Rare:64 | ||||
| chr21:25734844-25735090 | Common:2; Rare:103 | ||||
| chr21:25735098-25735480 | Common:3; Rare:112 | ||||
| chr21:25735531-25735928 | Common:4; Rare:101 | ||||
| chr21:26845401-26845555 | Common:1; Rare:38 | ||||
| chr21:28992797-28993152 | Common:2; Rare:146 | ||||
| chr21:29019297-29019416 | Common:5; Rare:50 | ||||
| chr21:29024526-29024759 | Common:2; Rare:101 | ||||
| chr21:29024876-29025043 | Rare:32 | ||||
| chr21:31659502-31659838 | Common:2; Rare:151; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 |