| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:31160481-31160714 | Rare:40 | ||||
| chr21:36135562-36135593 | Rare:4 | ||||
| chr21:44866822-44867111 | Common:3; Rare:46 | ||||
| chr21:45491139-45491305 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr21:45590509-45590795 | Common:6; Rare:95 | ||||
| chr21:45984131-45984550 | Common:6; Rare:146; Clinvar:17; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr21:45989984-45990284 | Common:4; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:45992160-45992397 | Common:1; Rare:81; Clinvar:10; Clinvar (benign):3 | ||||
| chr21:46122070-46122158 | Common:2; Rare:39; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr21:46125147-46125311 | Common:1; Rare:70; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr21:46125780-46126536 | Common:12; Rare:389; Clinvar:49; Clinvar (benign):33; Clinvar (pathogenic):5 | ||||
| chr21:46130873-46131170 | Common:7; Rare:124 | ||||
| chr21:46131825-46132010 | Common:1; Rare:93; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr22:18068504-18068603 | Common:2; Rare:14 | ||||
| chr22:19171606-19171724 | Rare:37 |