| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45365852-45365898 | Rare:7 | ||||
| chr21:45367000-45367333 | Common:7; Rare:74 | ||||
| chr21:45406207-45406719 | Common:2; Rare:98 | ||||
| chr21:45439126-45439289 | Common:3; Rare:42 | ||||
| chr21:45481861-45482020 | Rare:57; Clinvar:1 | ||||
| chr21:45508198-45508558 | Common:4; Rare:136 | ||||
| chr21:45510841-45511226 | Common:33; Rare:142; Clinvar (benign):4 | ||||
| chr21:45517840-45518063 | Common:1; Rare:36 | ||||
| chr21:45519243-45519535 | Common:4; Rare:51 | ||||
| chr21:45530282-45530370 | Common:2; Rare:35 | ||||
| chr21:45555002-45555296 | Common:23; Rare:106 | ||||
| chr21:45786114-45786284 | Common:3; Rare:35 | ||||
| chr21:45989603-45989775 | Common:1; Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chr21:46227046-46227233 | Common:2; Rare:28 | ||||
| chr21:46241964-46241996 | Common:2; Rare:3 |