Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2336424-2336551 | Rare:50 | ||||
chr17:2511804-2511944 | Common:2; Rare:41 | ||||
chr17:2593489-2593664 | Common:2; Rare:65 | ||||
chr17:2593818-2594001 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):3 | ||||
chr17:3636241-3636511 | Common:4; Rare:76; Clinvar (benign):1 | ||||
chr17:3668533-3668829 | Common:3; Rare:118 | ||||
chr17:3723764-3723925 | Common:1; Rare:89 | ||||
chr17:3892952-3893274 | Common:3; Rare:109 | ||||
chr17:4143001-4143250 | Rare:82 | ||||
chr17:4143597-4143727 | Common:4; Rare:72 | ||||
chr17:4263937-4264024 | Rare:38 | ||||
chr17:4555304-4555513 | Common:3; Rare:96 | ||||
chr17:4704092-4704260 | Rare:84 | ||||
chr17:4731400-4731481 | Common:2; Rare:31 | ||||
chr17:4738460-4738667 | Common:1; Rare:40 |