Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228292387-228292681 | Common:1; Rare:76; Clinvar (benign):1 | ||||
chr1:229432252-229432884 | Common:4; Rare:140; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
chr1:234600055-234600297 | Common:7; Rare:103 | ||||
chr10:10798373-10798475 | Common:3; Rare:18 | ||||
chr10:14371675-14371994 | Common:2; Rare:50 | ||||
chr10:24118390-24118537 | Rare:36 | ||||
chr10:26939762-26939880 | Common:2; Rare:15 | ||||
chr10:38402865-38403241 | Common:17; Rare:142 | ||||
chr10:46786778-46786874 | Rare:7 | ||||
chr10:47553488-47553590 | Rare:12 | ||||
chr10:73247208-73247357 | Rare:80 | ||||
chr10:73730470-73730595 | Rare:30 | ||||
chr10:79826239-79826417 | Common:3; Rare:56 | ||||
chr10:86666656-86666829 | Rare:45 | ||||
chr10:87342264-87342406 | Common:3; Rare:45 |