Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25337779-25338002 | Rare:30 | ||||
chr1:25338297-25338516 | Common:2; Rare:75 | ||||
chr1:25338846-25338881 | Common:1; Rare:4 | ||||
chr1:25430193-25430344 | Common:4; Rare:46 | ||||
chr1:25430616-25431011 | Common:4; Rare:120 | ||||
chr1:25799955-25800302 | Common:2; Rare:114; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):4 | ||||
chr1:25800569-25800668 | Rare:21 | ||||
chr1:25819829-25820013 | Common:4; Rare:58 | ||||
chr1:25820095-25820243 | Common:1; Rare:40 | ||||
chr1:25820790-25821056 | Common:5; Rare:54 | ||||
chr1:25859362-25859595 | Common:3; Rare:96 | ||||
chr1:25904962-25905229 | Rare:43 | ||||
chr1:25998095-25998408 | Common:2; Rare:81 | ||||
chr1:26110977-26111165 | Common:2; Rare:62 | ||||
chr1:26111668-26111860 | Common:1; Rare:70 |