Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15847457-15847711 | Rare:91 | ||||
chr1:16237137-16237291 | Common:1; Rare:54 | ||||
chr1:16352413-16352606 | Common:3; Rare:105 | ||||
chr1:16440524-16440774 | Common:2; Rare:71 | ||||
chr1:16613435-16613703 | Common:4; Rare:1 | ||||
chr1:16740158-16740299 | |||||
chr1:17053943-17054331 | Common:3; Rare:123; Clinvar:17; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
chr1:17119430-17119571 | Rare:33 | ||||
chr1:17439281-17439405 | Common:1; Rare:26 | ||||
chr1:17439652-17439909 | Rare:85 | ||||
chr1:17539573-17539919 | Rare:80 | ||||
chr1:19210211-19210533 | Common:1; Rare:106 | ||||
chr1:19251479-19251946 | Common:9; Rare:162 | ||||
chr1:19311910-19312343 | Common:9; Rare:196 | ||||
chr1:19485454-19485775 | Rare:120 |