Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24413684-24413882 | Common:1; Rare:47 | ||||
chr1:24642911-24643335 | Common:2; Rare:140 | ||||
chr1:25232444-25232648 | Rare:83 | ||||
chr1:25247431-25247621 | Common:2; Rare:66 | ||||
chr1:25338190-25338494 | Common:2; Rare:102 | ||||
chr1:25819769-25820013 | Common:4; Rare:80 | ||||
chr1:25859351-25859580 | Common:3; Rare:97 | ||||
chr1:25906397-25906591 | Rare:76 | ||||
chr1:26279844-26280203 | Rare:192 | ||||
chr1:26432119-26432414 | Common:4; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26890244-26890325 | Common:1; Rare:36 | ||||
chr1:26900438-26900524 | Rare:33 | ||||
chr1:26921577-26921887 | Common:3; Rare:95 | ||||
chr1:27322079-27322299 | Common:1; Rare:79 | ||||
chr1:27392461-27392675 | Common:1; Rare:71 |