Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:67717677-67717972 | Common:2; Rare:101 | ||||
chr17:68247813-68248114 | Common:5; Rare:137 | ||||
chr17:68511871-68512000 | Rare:30 | ||||
chr17:68512273-68512489 | Common:1; Rare:72; Clinvar (benign):1 | ||||
chr17:68513124-68513439 | Common:3; Rare:96 | ||||
chr17:69327113-69327339 | Common:1; Rare:71 | ||||
chr17:73192819-73193076 | Common:15; Rare:101; Clinvar:2; Clinvar (benign):1 | ||||
chr17:73232246-73232710 | Common:3; Rare:163 | ||||
chr17:74466590-74466692 | Rare:33 | ||||
chr17:74776240-74776503 | Common:4; Rare:83 | ||||
chr17:75012551-75012824 | Common:2; Rare:83 | ||||
chr17:75046945-75047188 | Common:1; Rare:71 | ||||
chr17:75182942-75183227 | Common:1; Rare:87 | ||||
chr17:75205356-75205767 | Common:1; Rare:136 | ||||
chr17:75261556-75261935 | Common:4; Rare:122; Clinvar (benign):2 |