Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:229431431-229431911 | Common:1; Rare:122; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
chr1:229431992-229432467 | Common:1; Rare:104; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
chr1:234600012-234600297 | Common:7; Rare:118 | ||||
chr1:246569745-246569899 | Common:1; Rare:29 | ||||
chr10:5524815-5524972 | Common:1; Rare:45 | ||||
chr10:21495776-21496007 | Common:1; Rare:96 | ||||
chr10:29409417-29409616 | Common:2; Rare:59 | ||||
chr10:46786767-46786874 | Rare:9 | ||||
chr10:47553484-47553569 | Rare:6 | ||||
chr10:73247191-73247357 | Rare:91 | ||||
chr10:73653797-73654067 | Common:1; Rare:54 | ||||
chr10:73730452-73730585 | Common:1; Rare:36 | ||||
chr10:86666617-86666831 | Rare:52 | ||||
chr10:86755801-86755908 | Rare:32 | ||||
chr10:86971176-86971219 | Rare:12 |