Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11805921-11806249 | Common:2; Rare:86; Clinvar:1 | ||||
chr1:11980405-11980462 | Common:1; Rare:20; Clinvar (benign):1 | ||||
chr1:12125832-12126012 | Common:2; Rare:52 | ||||
chr1:12166838-12167068 | Common:4; Rare:69 | ||||
chr1:12617276-12617378 | Rare:27 | ||||
chr1:15410154-15410275 | Rare:35 | ||||
chr1:16352401-16352591 | Common:3; Rare:105 | ||||
chr1:17438432-17438738 | Common:2; Rare:121 | ||||
chr1:19210243-19210460 | Rare:80 | ||||
chr1:19251520-19251838 | Common:6; Rare:101 | ||||
chr1:19485437-19485741 | Common:1; Rare:103 | ||||
chr1:19596672-19597052 | Common:3; Rare:121 | ||||
chr1:20588743-20588996 | Common:3; Rare:40 | ||||
chr1:21345493-21345640 | Rare:56 | ||||
chr1:23019328-23019558 | Rare:80 |