Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234600055-234600309 | Common:7; Rare:107 | ||||
chr1:234610174-234610320 | Common:2; Rare:58 | ||||
chr1:234611362-234611446 | Common:1; Rare:27 | ||||
chr1:234657088-234657459 | Common:2; Rare:63 | ||||
chr1:235458668-235458888 | Rare:58; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:244451132-244451264 | Common:2; Rare:38 | ||||
chr1:244863736-244863839 | Rare:35; Clinvar:1; Clinvar (benign):2 | ||||
chr1:246569669-246569876 | Common:1; Rare:38 | ||||
chr10:5525856-5526118 | Common:5; Rare:59 | ||||
chr10:5768213-5768652 | Common:1; Rare:90 | ||||
chr10:6163635-6163887 | Common:6; Rare:89 | ||||
chr10:13125887-13126015 | Rare:44; Clinvar (pathogenic):1 | ||||
chr10:24255139-24255491 | Common:1; Rare:68 | ||||
chr10:28078246-28078325 | Rare:15 | ||||
chr10:28120322-28120630 | Common:2; Rare:72 |