Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15152434-15152632 | Rare:28 | ||||
chr1:15152650-15152870 | Common:6; Rare:47 | ||||
chr1:15153564-15153797 | Common:3; Rare:61 | ||||
chr1:15154184-15154304 | Rare:25 | ||||
chr1:15246917-15247298 | Common:7; Rare:107 | ||||
chr1:15409766-15409984 | Common:1; Rare:68 | ||||
chr1:15525332-15525472 | Rare:31 | ||||
chr1:15526438-15526990 | Common:2; Rare:159 | ||||
chr1:15617145-15617534 | Common:2; Rare:106 | ||||
chr1:15684245-15684368 | Common:1; Rare:38 | ||||
chr1:15847465-15847610 | Rare:54 | ||||
chr1:15847742-15847886 | Rare:48 | ||||
chr1:15976062-15976216 | Common:2; Rare:42 | ||||
chr1:16026905-16027019 | Common:3; Rare:37 | ||||
chr1:16048820-16049120 | Common:2; Rare:110; Clinvar (benign):1 |