Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10032763-10032959 | Rare:51 | ||||
chr1:10398896-10399103 | Common:2; Rare:81 | ||||
chr1:10430392-10430502 | Common:3; Rare:39 | ||||
chr1:10430654-10430756 | Common:5; Rare:37 | ||||
chr1:11262506-11262867 | Common:3; Rare:106 | ||||
chr1:11805905-11806265 | Common:2; Rare:100; Clinvar:1 | ||||
chr1:11980104-11980299 | Common:3; Rare:59; Clinvar (benign):1 | ||||
chr1:12618207-12618417 | Rare:41 | ||||
chr1:13749143-13749451 | Common:2; Rare:105 | ||||
chr1:16352420-16352587 | Common:3; Rare:88 | ||||
chr1:19210213-19210401 | Rare:72 | ||||
chr1:19251506-19251857 | Common:6; Rare:117 | ||||
chr1:19312028-19312333 | Common:8; Rare:150 | ||||
chr1:20661326-20661736 | Common:3; Rare:151; Clinvar:4; Clinvar (benign):6 | ||||
chr1:20786602-20786856 | Rare:95 |