| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45353086-45353386 | Rare:65 | ||||
| chr21:45478572-45478784 | Common:4; Rare:65 | ||||
| chr21:45486674-45486897 | Common:4; Rare:54; Clinvar:1 | ||||
| chr21:45991913-45992072 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr21:45992160-45992397 | Common:1; Rare:81; Clinvar:10; Clinvar (benign):3 | ||||
| chr21:45998132-45998425 | Common:1; Rare:103; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr21:46116156-46116403 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:46240953-46241145 | Rare:55 | ||||
| chr21:46242845-46243045 | Common:5; Rare:51 | ||||
| chr21:46254447-46254696 | Common:1; Rare:59 | ||||
| chr21:46261311-46261652 | Common:2; Rare:98 | ||||
| chr21:46266158-46266319 | Common:3; Rare:41 | ||||
| chr21:46437886-46438256 | Rare:93; Clinvar:4 | ||||
| chr21:46484563-46484826 | Common:3; Rare:43 | ||||
| chr22:17037121-17037292 | Common:1; Rare:38 |