| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:34888001-34888155 | Common:1; Rare:34 | ||||
| chr21:36005238-36005320 | Rare:17 | ||||
| chr21:36135537-36135692 | Common:1; Rare:30 | ||||
| chr21:37221313-37221457 | Common:1; Rare:65 | ||||
| chr21:41951644-41951876 | Common:1; Rare:39 | ||||
| chr21:41952131-41952346 | Rare:45 | ||||
| chr21:42534396-42534525 | Common:1; Rare:25 | ||||
| chr21:42534634-42534786 | Common:1; Rare:39 | ||||
| chr21:45349916-45350132 | Common:1; Rare:36 | ||||
| chr21:45984047-45984446 | Common:4; Rare:122; Clinvar:17; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr21:45992188-45992397 | Common:1; Rare:71; Clinvar:8; Clinvar (benign):3 | ||||
| chr21:46429908-46430027 | Common:1; Rare:49 | ||||
| chr22:17037150-17037302 | Common:3; Rare:32 | ||||
| chr22:17639581-17639903 | Common:5; Rare:84 | ||||
| chr22:19576858-19577021 | Common:2; Rare:27 |