| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44299974-44300141 | Common:1; Rare:62; Clinvar (benign):1 | ||||
| chr21:44801729-44801897 | Rare:71 | ||||
| chr21:44817964-44818237 | Common:1; Rare:112 | ||||
| chr21:44873506-44873792 | Common:3; Rare:111 | ||||
| chr21:44939874-44940042 | Common:2; Rare:47 | ||||
| chr21:45287875-45288085 | Common:6; Rare:83 | ||||
| chr21:45981513-45981831 | Common:23; Rare:72; Clinvar (benign):2 | ||||
| chr21:46184423-46184724 | Common:3; Rare:26 | ||||
| chr21:46286222-46286396 | Common:4; Rare:66 | ||||
| chr21:46323830-46324224 | Common:3; Rare:145; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46431364-46431641 | Rare:94; Clinvar:1; Clinvar (benign):4 | ||||
| chr21:46458680-46459072 | Common:3; Rare:134 | ||||
| chr22:17084791-17084972 | Common:2; Rare:63; Clinvar:1 | ||||
| chr22:17159194-17159393 | Common:5; Rare:100 | ||||
| chr22:17628712-17628866 | Common:1; Rare:49 |