Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32893321-32893384 | Rare:7 | ||||
chr1:32893411-32893571 | Rare:45 | ||||
chr1:32893577-32893815 | Common:1; Rare:71 | ||||
chr1:33036814-33037082 | Rare:101; Clinvar (pathogenic):1 | ||||
chr1:33080992-33081209 | Common:2; Rare:66 | ||||
chr1:33472357-33472671 | Rare:70 | ||||
chr1:34165048-34165380 | Common:3; Rare:71 | ||||
chr1:34165790-34165920 | Rare:35 | ||||
chr1:34985301-34985456 | Common:2; Rare:47 | ||||
chr1:35031668-35032011 | Common:1; Rare:100 | ||||
chr1:35192688-35192723 | Rare:13 | ||||
chr1:35193022-35193036 | Rare:3 | ||||
chr1:35193047-35193212 | Rare:73 | ||||
chr1:35268637-35269037 | Rare:141 | ||||
chr1:35557362-35557451 | Rare:21 |