Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43649864-43650201 | Rare:82 | ||||
chr1:43650233-43650513 | Rare:61 | ||||
chr1:43707351-43707576 | Common:2; Rare:65 | ||||
chr1:43979061-43979305 | Common:2; Rare:86 | ||||
chr1:43979880-43979961 | Rare:21 | ||||
chr1:44674433-44674759 | Common:3; Rare:81 | ||||
chr1:44775480-44775604 | Rare:48 | ||||
chr1:44986538-44986791 | Common:2; Rare:49; Clinvar (benign):1 | ||||
chr1:45011266-45011382 | Rare:30 | ||||
chr1:45339996-45340266 | Rare:97; Clinvar:13; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:45340388-45340576 | Common:1; Rare:46; Clinvar:1 | ||||
chr1:45499997-45500361 | Common:2; Rare:83; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:45687027-45687289 | Common:2; Rare:74 | ||||
chr1:45688049-45688243 | Common:1; Rare:54 | ||||
chr1:46132615-46132722 | Rare:40 |