| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44873503-44873620 | Rare:35 | ||||
| chr21:44873626-44874050 | Common:8; Rare:170 | ||||
| chr21:45287861-45288108 | Common:6; Rare:97 | ||||
| chr21:45981549-45981914 | Common:24; Rare:92; Clinvar:3; Clinvar (benign):3 | ||||
| chr21:45981917-45981946 | Rare:10; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46001959-46002401 | Common:2; Rare:153; Clinvar:19; Clinvar (benign):15; Clinvar (pathogenic):1 | ||||
| chr21:46097830-46098166 | Common:4; Rare:103; Clinvar (benign):1 | ||||
| chr21:46286256-46286407 | Common:4; Rare:56 | ||||
| chr21:46286541-46286688 | Common:1; Rare:43 | ||||
| chr21:46323830-46324202 | Common:2; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46635330-46635726 | Common:10; Rare:146 | ||||
| chr22:17159197-17159375 | Common:4; Rare:83 | ||||
| chr22:17628680-17628866 | Common:1; Rare:64 | ||||
| chr22:17638677-17638819 | Rare:49 | ||||
| chr22:18077819-18078007 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):1 |