Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:36060503-36060570 | Common:1; Rare:22 | ||||
chr21:37073040-37073348 | Common:5; Rare:122 | ||||
chr21:39387650-39387808 | Common:2; Rare:69 | ||||
chr21:42893066-42893328 | Common:4; Rare:85 | ||||
chr21:44873657-44874050 | Common:8; Rare:153 | ||||
chr21:45287879-45288085 | Common:5; Rare:80 | ||||
chr21:45981529-45981813 | Common:23; Rare:63; Clinvar (benign):2 | ||||
chr21:46323830-46324153 | Common:2; Rare:108; Clinvar (benign):1 | ||||
chr21:46635474-46635689 | Common:4; Rare:68 | ||||
chr22:17159207-17159368 | Common:4; Rare:75 | ||||
chr22:17638693-17638760 | Rare:19 | ||||
chr22:19432303-19432567 | Common:3; Rare:106 | ||||
chr22:20117259-20117571 | Common:2; Rare:96 | ||||
chr22:21002106-21002195 | Common:3; Rare:26 | ||||
chr22:24555735-24556061 | Rare:101 |