Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156125246-156125334 | Rare:11 | ||||
chr1:156130304-156130764 | Common:3; Rare:113; Clinvar:10; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
chr1:156456524-156456774 | Rare:57 | ||||
chr1:156502945-156503094 | Common:1; Rare:32 | ||||
chr1:156503367-156503589 | Common:1; Rare:39 | ||||
chr1:156563645-156563796 | Common:1; Rare:51 | ||||
chr1:156657546-156657684 | Rare:41 | ||||
chr1:156660040-156660404 | Common:2; Rare:68 | ||||
chr1:156660428-156660474 | Rare:11 | ||||
chr1:156661355-156661590 | Common:1; Rare:40 | ||||
chr1:156748379-156748458 | Common:1; Rare:16 | ||||
chr1:156748915-156749057 | Common:1; Rare:26 | ||||
chr1:158019675-158019761 | Common:1; Rare:21 | ||||
chr1:161115361-161115494 | Rare:25 | ||||
chr1:161133259-161133278 | Rare:3 |