Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16613453-16613890 | Common:7; Rare:1 | ||||
chr1:16980440-16980950 | Common:6; Rare:133 | ||||
chr1:17011895-17012169 | Common:2; Rare:70; Clinvar:1 | ||||
chr1:17054104-17054395 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
chr1:17119448-17119602 | Rare:43 | ||||
chr1:17439647-17439999 | Rare:113 | ||||
chr1:17539744-17540144 | Common:2; Rare:207 | ||||
chr1:17540238-17540475 | Common:3; Rare:45 | ||||
chr1:18480786-18481017 | Common:2; Rare:45 | ||||
chr1:18902528-18903055 | Common:8; Rare:149; Clinvar:8 | ||||
chr1:18956624-18956949 | Common:3; Rare:85 | ||||
chr1:19210228-19210642 | Common:1; Rare:124 | ||||
chr1:19251476-19251842 | Common:6; Rare:126 | ||||
chr1:19312057-19312361 | Common:8; Rare:144 | ||||
chr1:19485475-19485829 | Rare:136 |