| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44012217-44012486 | Common:1; Rare:90 | ||||
| chr21:44299927-44300096 | Common:1; Rare:66 | ||||
| chr21:44801714-44801883 | Rare:67 | ||||
| chr21:44817959-44818253 | Common:1; Rare:122 | ||||
| chr21:44865147-44865416 | Common:2; Rare:72 | ||||
| chr21:44873632-44874080 | Common:9; Rare:172 | ||||
| chr21:44939920-44940049 | Common:1; Rare:38 | ||||
| chr21:45287883-45288087 | Common:5; Rare:79 | ||||
| chr21:45542418-45542544 | Rare:43 | ||||
| chr21:46286226-46286399 | Common:4; Rare:64 | ||||
| chr21:46286460-46286644 | Common:1; Rare:55 | ||||
| chr21:46323801-46324193 | Common:2; Rare:139; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46458671-46459055 | Common:3; Rare:130 | ||||
| chr21:46635355-46635747 | Common:8; Rare:143 | ||||
| chr22:17159223-17159373 | Common:4; Rare:70 |