| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45986674-45986997 | Common:5; Rare:108; Clinvar:12; Clinvar (benign):9 | ||||
| chr21:45987017-45987175 | Common:1; Rare:60; Clinvar:9; Clinvar (benign):4 | ||||
| chr21:46184409-46184753 | Common:4; Rare:32 | ||||
| chr21:46228631-46228926 | Common:3; Rare:134 | ||||
| chr21:46286215-46286399 | Common:4; Rare:70 | ||||
| chr21:46323837-46324199 | Common:2; Rare:124; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46605011-46605219 | Common:2; Rare:42 | ||||
| chr21:46605240-46605272 | Rare:8 | ||||
| chr22:17563276-17563625 | Common:2; Rare:74 | ||||
| chr22:17628693-17628860 | Common:1; Rare:55 | ||||
| chr22:17638689-17638817 | Rare:45 | ||||
| chr22:17774386-17774542 | Rare:52 | ||||
| chr22:18077829-18078050 | Common:4; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19122382-19122674 | Common:4; Rare:71 | ||||
| chr22:19178497-19178582 | Rare:19 |