| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39314317-39314533 | Common:2; Rare:97 | ||||
| chr21:39348569-39348734 | Common:1; Rare:66 | ||||
| chr21:39349073-39349453 | Common:18; Rare:113 | ||||
| chr21:39380172-39380487 | Common:1; Rare:145 | ||||
| chr21:39387512-39387802 | Common:2; Rare:101 | ||||
| chr21:39445731-39445955 | Common:3; Rare:69 | ||||
| chr21:39451612-39452012 | Common:3; Rare:160 | ||||
| chr21:39556120-39556460 | Rare:54 | ||||
| chr21:39612592-39612949 | Rare:93 | ||||
| chr21:41167802-41167992 | Common:1; Rare:38 | ||||
| chr21:41420201-41420701 | Common:13; Rare:339 | ||||
| chr21:41766922-41767322 | Common:10; Rare:172; Clinvar:2; Clinvar (benign):2 | ||||
| chr21:41953466-41953866 | Common:2; Rare:159 | ||||
| chr21:41953890-41954270 | Common:4; Rare:128 | ||||
| chr21:42009874-42010145 | Rare:114 |