| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:38605326-38605550 | Common:1; Rare:42 | ||||
| chr21:41189570-41189887 | Common:1; Rare:53 | ||||
| chr21:45486591-45486992 | Common:5; Rare:105; Clinvar:4 | ||||
| chr21:45487307-45487515 | Common:3; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:45496417-45496560 | Common:1; Rare:56 | ||||
| chr21:45509075-45509447 | Common:4; Rare:137; Clinvar (benign):1 | ||||
| chr21:46118492-46118669 | Common:2; Rare:65; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr21:46124866-46124948 | Common:1; Rare:51; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr21:46130000-46130439 | Common:5; Rare:157 | ||||
| chr22:16601159-16601390 | Common:1; Rare:86 | ||||
| chr22:18068506-18068553 | Rare:5 | ||||
| chr22:19985422-19985475 | Rare:15 | ||||
| chr22:22298058-22298196 | Common:2; Rare:50 | ||||
| chr22:26672453-26672955 | Common:5; Rare:117 | ||||
| chr22:28799125-28799416 | Rare:53 |