Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40040433-40040791 | Common:3; Rare:106 | ||||
chr1:40161152-40161402 | Common:1; Rare:66 | ||||
chr1:40257915-40258264 | Common:4; Rare:94; Clinvar:7 | ||||
chr1:40508681-40508812 | Common:4; Rare:36 | ||||
chr1:40691756-40691805 | Rare:20 | ||||
chr1:41242105-41242377 | Rare:79 | ||||
chr1:42456010-42456103 | Rare:31 | ||||
chr1:42682608-42682655 | Rare:23 | ||||
chr1:42766603-42766722 | Rare:26; Clinvar:1; Clinvar (benign):1 | ||||
chr1:42766996-42767303 | Common:4; Rare:102; Clinvar (benign):1 | ||||
chr1:42817004-42817136 | Common:1; Rare:32 | ||||
chr1:42817236-42817577 | Rare:114 | ||||
chr1:42846412-42846636 | Common:1; Rare:60 | ||||
chr1:42958839-42959035 | Common:2; Rare:48; Clinvar:3; Clinvar (benign):3 | ||||
chr1:43358701-43358983 | Common:7; Rare:88 |