Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:44739641-44739873 | Common:2; Rare:88 | ||||
chr1:44775445-44775613 | Rare:65 | ||||
chr1:45010961-45011218 | Common:2; Rare:69 | ||||
chr1:45012178-45012278 | Rare:38; Clinvar:4 | ||||
chr1:45326635-45326904 | Rare:58 | ||||
chr1:45339959-45340077 | Rare:37 | ||||
chr1:45340103-45340243 | Rare:61; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:45340329-45340574 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
chr1:45500085-45500351 | Common:1; Rare:68; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45521860-45522087 | Common:1; Rare:88 | ||||
chr1:45550730-45551148 | Common:3; Rare:97 | ||||
chr1:45566588-45566902 | Common:5; Rare:88 | ||||
chr1:45583772-45584060 | Common:1; Rare:91 | ||||
chr1:45687059-45687408 | Common:1; Rare:92 | ||||
chr1:45688055-45688216 | Common:1; Rare:41 |