Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11805907-11806324 | Common:2; Rare:120; Clinvar:1 | ||||
chr1:12618207-12618476 | Common:1; Rare:56 | ||||
chr1:15758262-15758842 | Common:1; Rare:110 | ||||
chr1:16156011-16156191 | Rare:36; Clinvar:2 | ||||
chr1:19210259-19210508 | Rare:87 | ||||
chr1:19251518-19251824 | Common:6; Rare:95 | ||||
chr1:19312089-19312350 | Common:5; Rare:121 | ||||
chr1:19485445-19485765 | Rare:120 | ||||
chr1:20685138-20685364 | Common:2; Rare:38 | ||||
chr1:23778281-23778446 | Common:6; Rare:84 | ||||
chr1:23791066-23791247 | Rare:55 | ||||
chr1:23959644-23959854 | Common:2; Rare:54 | ||||
chr1:25232460-25232642 | Rare:72 | ||||
chr1:25247451-25247617 | Common:2; Rare:54 | ||||
chr1:26432108-26432428 | Common:5; Rare:86; Clinvar:2; Clinvar (benign):1 |