Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:43332104-43332288 | Rare:40 | ||||
chr21:45992188-45992397 | Common:1; Rare:71; Clinvar:8; Clinvar (benign):3 | ||||
chr22:17037166-17037284 | Common:1; Rare:27 | ||||
chr22:17866181-17866495 | Rare:61 | ||||
chr22:18970327-18970542 | Common:4; Rare:74 | ||||
chr22:20703116-20703459 | Common:1; Rare:93 | ||||
chr22:21014238-21014444 | Rare:55 | ||||
chr22:21102922-21103034 | Rare:27 | ||||
chr22:22298024-22298210 | Common:7; Rare:82 | ||||
chr22:25447951-25448147 | Common:3; Rare:69 | ||||
chr22:29478096-29478254 | Common:1; Rare:30 | ||||
chr22:30922240-30922361 | Common:1; Rare:48 | ||||
chr22:32857006-32857360 | Common:3; Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
chr22:35895025-35895123 | Rare:26 | ||||
chr22:39521555-39521813 | Common:1; Rare:126 |