Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:41026161-41026192 | Common:1; Rare:6 | ||||
chr17:41108116-41108340 | Common:7; Rare:54 | ||||
chr17:41822138-41822280 | Rare:44; Clinvar:1 | ||||
chr17:42422889-42422989 | Rare:35; Clinvar:2 | ||||
chr17:45149287-45149391 | Rare:37 | ||||
chr17:45150142-45150301 | Rare:64 | ||||
chr17:45247749-45247963 | Common:1; Rare:41 | ||||
chr17:50197729-50198005 | Common:4; Rare:74; Clinvar:2; Clinvar (benign):6 | ||||
chr17:58324405-58324530 | Rare:38 | ||||
chr17:64500062-64500690 | Common:1; Rare:195 | ||||
chr17:76345565-76345660 | Common:1; Rare:15 | ||||
chr17:76557631-76557815 | Common:1; Rare:67 | ||||
chr18:5238030-5238130 | Common:1; Rare:40 | ||||
chr18:11852502-11852577 | Rare:26 | ||||
chr18:28177957-28178168 | Common:2; Rare:87 |