Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20656121-20656279 | Common:1; Rare:40; Clinvar (benign):1 | ||||
chr1:21827861-21828044 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
chr1:21875866-21876313 | Common:1; Rare:138; Clinvar:6; Clinvar (benign):1 | ||||
chr1:21884856-21885152 | Common:1; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
chr1:22025450-22025567 | Common:5; Rare:41 | ||||
chr1:22254814-22255007 | Rare:44 | ||||
chr1:22660612-22660825 | Rare:37 | ||||
chr1:23397582-23397914 | Common:1; Rare:105 | ||||
chr1:23748862-23749077 | Common:1; Rare:43 | ||||
chr1:23755678-23755946 | Common:5; Rare:64 | ||||
chr1:23756249-23756280 | Rare:4 | ||||
chr1:24321914-24321976 | Common:1; Rare:7 | ||||
chr1:25875503-25875765 | Rare:69 | ||||
chr1:27355662-27355856 | Common:1; Rare:50; Clinvar (pathogenic):1 | ||||
chr1:27625395-27625488 | Rare:19 |