| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63488290-63488790 | Common:6; Rare:123; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr20:63785657-63786057 | Common:3; Rare:84 | ||||
| chr20:63834980-63835390 | Rare:92 | ||||
| chr20:63858952-63859352 | Rare:109 | ||||
| chr20:63957242-63957642 | Rare:164 | ||||
| chr20:63978707-63979107 | Common:4; Rare:153 | ||||
| chr20:64160786-64161346 | Common:15; Rare:258 | ||||
| chr20:64161977-64162137 | Common:1; Rare:37 | ||||
| chr20:64162590-64162746 | Common:1; Rare:33 | ||||
| chr21:6368986-6369108 | Rare:4 | ||||
| chr21:6369502-6370228 | Rare:13 | ||||
| chr21:13923312-13923492 | Rare:46 | ||||
| chr21:14027274-14027474 | Common:3; Rare:61 | ||||
| chr21:14080460-14080860 | Common:12; Rare:146 | ||||
| chr21:14384371-14384771 | Rare:79 |