Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:232950235-232950297 | Common:1; Rare:12 | ||||
chr1:232950317-232950711 | Common:6; Rare:126 | ||||
chr1:233295662-233295809 | Common:1; Rare:46 | ||||
chr1:233613917-233614260 | Common:5; Rare:108 | ||||
chr1:234373032-234373941 | Common:6; Rare:321; Clinvar (benign):10 | ||||
chr1:234373990-234374061 | Rare:20 | ||||
chr1:234478549-234478636 | Common:1; Rare:39 | ||||
chr1:234479052-234479288 | Common:6; Rare:98 | ||||
chr1:234608191-234608631 | Common:2; Rare:188; Clinvar (benign):1 | ||||
chr1:234609270-234609428 | Common:1; Rare:40 | ||||
chr1:234609431-234609519 | Common:1; Rare:41 | ||||
chr1:234609869-234609992 | Rare:41 | ||||
chr1:235128737-235129130 | Common:1; Rare:160 | ||||
chr1:235160649-235160889 | Common:3; Rare:67 | ||||
chr1:235160934-235161065 | Common:1; Rare:44 |