Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:15125663-15125982 | Common:2; Rare:76 | ||||
chr19:15179186-15179397 | Common:2; Rare:65; Clinvar:1; Clinvar (benign):3 | ||||
chr19:15331867-15332204 | Common:2; Rare:106 | ||||
chr19:15508373-15508566 | Common:1; Rare:46 | ||||
chr19:16542416-16542612 | Common:2; Rare:54 | ||||
chr19:16660084-16660358 | Common:3; Rare:107 | ||||
chr19:17305687-17305904 | Common:2; Rare:96 | ||||
chr19:17337420-17337589 | Common:1; Rare:34 | ||||
chr19:17405576-17405822 | Common:5; Rare:40 | ||||
chr19:17795011-17795167 | Common:1; Rare:33 | ||||
chr19:18152983-18153292 | Common:1; Rare:100 | ||||
chr19:18280123-18280465 | Common:4; Rare:132 | ||||
chr19:18280690-18281067 | Rare:138 | ||||
chr19:18573188-18573402 | Rare:51 | ||||
chr19:18919344-18919763 | Common:3; Rare:154 |