| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44801761-44801876 | Rare:50 | ||||
| chr21:44873618-44874070 | Common:9; Rare:178 | ||||
| chr21:44928805-44928893 | Common:5; Rare:9 | ||||
| chr21:44939874-44940052 | Common:2; Rare:50 | ||||
| chr21:45073559-45073845 | Common:5; Rare:68 | ||||
| chr21:45287851-45288102 | Common:6; Rare:99 | ||||
| chr21:45981513-45981783 | Common:23; Rare:52; Clinvar (benign):1 | ||||
| chr21:46184423-46184741 | Common:4; Rare:29 | ||||
| chr21:46286285-46286402 | Common:2; Rare:36 | ||||
| chr21:46286562-46286684 | Common:1; Rare:39 | ||||
| chr21:46323801-46324224 | Common:3; Rare:161; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46458696-46459063 | Common:3; Rare:127 | ||||
| chr21:46635472-46635731 | Common:5; Rare:84 | ||||
| chr22:11066053-11066311 | |||||
| chr22:17159175-17159357 | Common:6; Rare:81 |