| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63864997-63865384 | Common:2; Rare:136 | ||||
| chr20:63956356-63956705 | Common:1; Rare:137 | ||||
| chr20:63979481-63979579 | Rare:24 | ||||
| chr20:63980971-63981297 | Common:4; Rare:105; Clinvar:7; Clinvar (benign):5 | ||||
| chr21:14383115-14383461 | Common:1; Rare:97 | ||||
| chr21:15064813-15065166 | Rare:116 | ||||
| chr21:17512468-17512663 | Common:3; Rare:45 | ||||
| chr21:17512860-17513148 | Common:1; Rare:100 | ||||
| chr21:17612816-17612918 | Common:1; Rare:43 | ||||
| chr21:17819327-17819488 | Common:1; Rare:57 | ||||
| chr21:25607458-25607555 | Rare:54 | ||||
| chr21:25734851-25735490 | Common:5; Rare:222 | ||||
| chr21:25735578-25735728 | Rare:45 | ||||
| chr21:25897571-25897855 | Common:1; Rare:92; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr21:26170565-26170928 | Common:6; Rare:117; Clinvar:5; Clinvar (benign):2 |