Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174159274-174159560 | Common:4; Rare:99 | ||||
chr1:174999300-174999510 | Common:2; Rare:54 | ||||
chr1:174999621-175000156 | Common:3; Rare:177 | ||||
chr1:178724935-178725335 | Common:12; Rare:134 | ||||
chr1:179293686-179293907 | Common:3; Rare:66 | ||||
chr1:179881992-179882307 | Common:4; Rare:74 | ||||
chr1:179882488-179882912 | Rare:212; Clinvar:9; Clinvar (benign):2 | ||||
chr1:179883016-179883109 | Common:3; Rare:37 | ||||
chr1:180154669-180154896 | Common:3; Rare:77 | ||||
chr1:181088494-181088707 | Rare:70 | ||||
chr1:182839566-182839744 | Common:2; Rare:82 | ||||
chr1:183472219-183472538 | Common:2; Rare:106 | ||||
chr1:183635589-183636114 | Common:5; Rare:142 | ||||
chr1:184051656-184051768 | Common:2; Rare:43 | ||||
chr1:185045250-185045632 | Common:2; Rare:132 |