Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15684961-15685218 | Common:2; Rare:40 | ||||
chr1:16352420-16352567 | Common:2; Rare:80 | ||||
chr1:17053924-17054368 | Common:3; Rare:138; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
chr1:17439652-17439868 | Rare:67 | ||||
chr1:19210248-19210530 | Common:1; Rare:93 | ||||
chr1:19251520-19251842 | Common:6; Rare:103 | ||||
chr1:19312089-19312333 | Common:5; Rare:116 | ||||
chr1:19485445-19485751 | Rare:108 | ||||
chr1:19596675-19597054 | Common:3; Rare:124 | ||||
chr1:20661360-20661707 | Common:3; Rare:126; Clinvar:4; Clinvar (benign):6 | ||||
chr1:21176830-21177146 | Rare:94 | ||||
chr1:21345502-21345636 | Rare:50 | ||||
chr1:21783070-21783277 | Common:2; Rare:76 | ||||
chr1:23743302-23743500 | Rare:77 | ||||
chr1:23778269-23778431 | Common:6; Rare:85 |