| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:16194263-16194573 | Common:2; Rare:86 | ||||
| chr21:16590221-16590314 | Rare:14 | ||||
| chr21:25729629-25729980 | Common:2; Rare:83 | ||||
| chr21:28090203-28090410 | Common:4; Rare:48 | ||||
| chr21:29002682-29002811 | Common:2; Rare:44 | ||||
| chr21:31667196-31667278 | Rare:16; Clinvar (pathogenic):3 | ||||
| chr21:32378895-32379182 | Rare:50 | ||||
| chr21:32448306-32448619 | Common:1; Rare:52 | ||||
| chr21:32451223-32451538 | Common:5; Rare:53 | ||||
| chr21:34827051-34827190 | Rare:14 | ||||
| chr21:37221350-37221444 | Rare:41 | ||||
| chr21:38351911-38352110 | Common:1; Rare:33 | ||||
| chr21:38503547-38503861 | Common:2; Rare:59 | ||||
| chr21:38539039-38539164 | Rare:37 | ||||
| chr21:38547128-38547437 | Common:3; Rare:57 |