Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26110971-26111226 | Common:2; Rare:89 | ||||
chr1:26112149-26112309 | Rare:42 | ||||
chr1:26234415-26234530 | Common:2; Rare:41 | ||||
chr1:26279941-26280163 | Rare:128 | ||||
chr1:26432091-26432433 | Common:5; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472102-26472627 | Common:5; Rare:171 | ||||
chr1:26473048-26473274 | Rare:119 | ||||
chr1:26529588-26529859 | Common:3; Rare:96 | ||||
chr1:26545696-26545870 | Common:1; Rare:35 | ||||
chr1:26695868-26696049 | Rare:59 | ||||
chr1:26787859-26788225 | Common:3; Rare:108; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26890211-26890359 | Common:1; Rare:54 | ||||
chr1:26900081-26900188 | Rare:39 | ||||
chr1:26900425-26900542 | Rare:42 | ||||
chr1:26921517-26921887 | Common:3; Rare:116 |