| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:41420300-41420650 | Common:5; Rare:139 | ||||
| chr21:41426135-41426246 | Common:1; Rare:24 | ||||
| chr21:41767032-41767193 | Common:7; Rare:136; Clinvar:2; Clinvar (benign):1 | ||||
| chr21:41879280-41879410 | Common:4; Rare:84 | ||||
| chr21:41953908-41954137 | Common:3; Rare:90 | ||||
| chr21:42009865-42010265 | Common:1; Rare:228 | ||||
| chr21:42010337-42010487 | Common:2; Rare:40 | ||||
| chr21:42878987-42879183 | Common:3; Rare:103 | ||||
| chr21:42879441-42879673 | Common:6; Rare:164 | ||||
| chr21:42892994-42893360 | Common:9; Rare:237 | ||||
| chr21:43659414-43659730 | Common:3; Rare:175 | ||||
| chr21:43718874-43719212 | Common:11; Rare:173 | ||||
| chr21:43719308-43719502 | Common:1; Rare:74 | ||||
| chr21:43728510-43729150 | Common:9; Rare:255 | ||||
| chr21:43776256-43776820 | Common:6; Rare:286; Clinvar:4; Clinvar (benign):16; Clinvar (pathogenic):2 |