| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63928297-63928356 | Rare:18 | ||||
| chr20:63930914-63931151 | Common:1; Rare:74; Clinvar:3; Clinvar (benign):6 | ||||
| chr20:63940453-63940775 | Rare:106 | ||||
| chr20:64076571-64076877 | Rare:85 | ||||
| chr20:64077161-64077306 | Rare:29 | ||||
| chr21:5086473-5086730 | Rare:23 | ||||
| chr21:5123780-5123841 | Rare:8 | ||||
| chr21:8849903-8850073 | Rare:17 | ||||
| chr21:14541631-14541865 | Common:2; Rare:41 | ||||
| chr21:17813496-17813714 | Common:1; Rare:41 | ||||
| chr21:25573972-25574044 | Rare:11 | ||||
| chr21:26844434-26844537 | Rare:37 | ||||
| chr21:26964473-26964729 | Common:2; Rare:50 | ||||
| chr21:26965337-26965599 | Common:2; Rare:91 | ||||
| chr21:26967580-26967806 | Common:3; Rare:61 |