| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44801739-44801890 | Rare:65 | ||||
| chr21:44873668-44874026 | Common:7; Rare:145 | ||||
| chr21:44939871-44940168 | Common:3; Rare:85 | ||||
| chr21:45287867-45288138 | Common:6; Rare:102 | ||||
| chr21:45981519-45981803 | Common:23; Rare:61; Clinvar (benign):2 | ||||
| chr21:46184378-46184758 | Common:5; Rare:37 | ||||
| chr21:46286237-46286402 | Common:4; Rare:61 | ||||
| chr21:46286574-46286651 | Common:1; Rare:22 | ||||
| chr21:46323809-46324177 | Common:2; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:17159141-17159389 | Common:7; Rare:118 | ||||
| chr22:17199626-17199669 | Common:1; Rare:11 | ||||
| chr22:17563269-17563498 | Common:2; Rare:45 | ||||
| chr22:17628675-17628925 | Common:1; Rare:97 | ||||
| chr22:17638684-17638817 | Rare:46 | ||||
| chr22:18024374-18024641 | Common:1; Rare:72 |