Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44739641-44739873 | Not yet | Common:2; Rare:88 | 271 | ||
chr1:44775445-44775613 | Not yet | Rare:65 | 204 | ||
chr1:45010961-45011218 | Not yet | Common:2; Rare:69 | 205 | ||
chr1:45012178-45012278 | Not yet | Rare:38; Clinvar:4 | 205 | ||
chr1:45326635-45326904 | Not yet | Rare:58 | 268 | ||
chr1:45339959-45340077 | Not yet | Rare:37 | 186 | ||
chr1:45340103-45340243 | Not yet | Rare:61; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | 131 | ||
chr1:45340329-45340574 | Not yet | Common:2; Rare:65; Clinvar:2; Clinvar (benign):1 | 276 | ||
chr1:45500085-45500351 | Not yet | Common:1; Rare:68; Clinvar:4; Clinvar (pathogenic):3 | 324 | ||
chr1:45521860-45522087 | Not yet | Common:1; Rare:88 | 241 | ||
chr1:45550730-45551148 | Not yet | Common:3; Rare:97 | 393 | ||
chr1:45566588-45566902 | Not yet | Common:5; Rare:88 | 399 | ||
chr1:45583772-45584060 | Not yet | Common:1; Rare:91 | 412 | ||
chr1:45687059-45687408 | Not yet | Common:1; Rare:92 | 341 | ||
chr1:45688055-45688216 | Not yet | Common:1; Rare:41 | 286 |