| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46115749-46115925 | Common:2; Rare:46; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr21:46116347-46116665 | Common:1; Rare:93; Clinvar:3; Clinvar (benign):3 | ||||
| chr21:46117203-46117451 | Common:3; Rare:79; Clinvar:3; Clinvar (benign):1 | ||||
| chr21:46118965-46119055 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr21:46229466-46229536 | Rare:17 | ||||
| chr21:46322862-46323146 | Common:2; Rare:79 | ||||
| chr21:46353863-46354066 | Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46416873-46416978 | Common:1; Rare:30 | ||||
| chr21:46439968-46440199 | Common:3; Rare:79; Clinvar:3; Clinvar (benign):5 | ||||
| chr21:46667375-46667409 | Common:1; Rare:7 | ||||
| chr22:10741991-10742135 | |||||
| chr22:12602003-12602307 | Rare:17 | ||||
| chr22:15642190-15642483 | Rare:21 | ||||
| chr22:16601047-16601488 | Common:2; Rare:165 | ||||
| chr22:16601693-16601958 | Common:1; Rare:102 |