Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42577660-42577869 | Common:1; Rare:104 | ||||
chr17:42609337-42609705 | Common:7; Rare:148; Clinvar (benign):1 | ||||
chr17:42833346-42833445 | Rare:31 | ||||
chr17:43125351-43125607 | Rare:48; Clinvar:3; Clinvar (benign):2 | ||||
chr17:43171000-43171236 | Rare:74 | ||||
chr17:44324774-44324958 | Common:2; Rare:66 | ||||
chr17:44899375-44899468 | Rare:39 | ||||
chr17:45060993-45061329 | Common:2; Rare:88 | ||||
chr17:48944788-48944918 | Common:2; Rare:36 | ||||
chr17:51260368-51260559 | Common:3; Rare:80 | ||||
chr17:54968631-54968727 | Common:3; Rare:56 | ||||
chr17:57850006-57850274 | Common:1; Rare:86 | ||||
chr17:59619538-59619949 | Common:3; Rare:148 | ||||
chr17:59707397-59707732 | Common:3; Rare:91; Clinvar (benign):3 | ||||
chr17:59892891-59893136 | Rare:71 |