Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25337779-25338002 | Not yet | Rare:30 | 175 | ||
chr1:25338297-25338516 | Not yet | Common:2; Rare:75 | 141 | ||
chr1:25338846-25338881 | Not yet | Common:1; Rare:4 | 16 | ||
chr1:25430193-25430344 | Not yet | Common:4; Rare:46 | 142 | ||
chr1:25430616-25431011 | Not yet | Common:4; Rare:120 | 201 | ||
chr1:25799955-25800302 | Not yet | Common:2; Rare:114; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):4 | 126 | ||
chr1:25800569-25800668 | Not yet | Rare:21 | 75 | ||
chr1:25819829-25820013 | Not yet | Common:4; Rare:58 | 104 | ||
chr1:25820095-25820243 | Not yet | Common:1; Rare:40 | 112 | ||
chr1:25820790-25821056 | Not yet | Common:5; Rare:54 | 146 | ||
chr1:25859362-25859595 | Not yet | Common:3; Rare:96 | 103 | ||
chr1:25904962-25905229 | Not yet | Rare:43 | 173 | ||
chr1:25998095-25998408 | Not yet | Common:2; Rare:81 | 157 | ||
chr1:26110977-26111165 | Not yet | Common:2; Rare:62 | 125 | ||
chr1:26111668-26111860 | Not yet | Common:1; Rare:70 | 109 |