Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:197201273-197201536 | Common:1; Rare:93 | ||||
chr1:204410481-204410518 | Common:1; Rare:10 | ||||
chr1:205729572-205729726 | Common:1; Rare:29 | ||||
chr1:222663103-222663289 | Rare:38 | ||||
chr1:222711479-222711636 | Rare:31 | ||||
chr1:223992564-223992760 | Common:3; Rare:73 | ||||
chr1:225512681-225512951 | Rare:63 | ||||
chr1:231422267-231422444 | Common:4; Rare:83; Clinvar:4; Clinvar (benign):3 | ||||
chr1:244863616-244863732 | Rare:44; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr10:13139808-13140002 | Rare:30 | ||||
chr10:15132889-15133084 | Common:2; Rare:48 | ||||
chr10:22437745-22437855 | Rare:19 | ||||
chr10:22437912-22438231 | Common:6; Rare:60 | ||||
chr10:24625022-24625295 | Common:6; Rare:36 | ||||
chr10:31468538-31468778 | Common:1; Rare:54 |