| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:15224352-15224702 | Common:2; Rare:78 | ||||
| chr21:15898032-15898231 | Common:1; Rare:35 | ||||
| chr21:17611481-17611763 | Common:5; Rare:67 | ||||
| chr21:17818290-17818402 | Rare:34 | ||||
| chr21:23391083-23391195 | Rare:21 | ||||
| chr21:25600447-25600567 | Rare:11 | ||||
| chr21:25865682-25865803 | Rare:25 | ||||
| chr21:25865888-25865944 | Rare:8 | ||||
| chr21:25891586-25891870 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr21:25898603-25898658 | Rare:17 | ||||
| chr21:25949112-25949222 | Rare:24 | ||||
| chr21:25949868-25950187 | Common:2; Rare:56 | ||||
| chr21:25950930-25951013 | Rare:16 | ||||
| chr21:25980602-25980895 | Common:8; Rare:55 | ||||
| chr21:26010244-26010518 | Common:1; Rare:30 |