Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:99970341-99970593 | Common:1; Rare:64 | ||||
chr1:100037818-100038260 | Common:1; Rare:148 | ||||
chr1:100038273-100038387 | Common:2; Rare:30 | ||||
chr1:100038470-100039025 | Common:6; Rare:165 | ||||
chr1:100132673-100132804 | Common:1; Rare:39 | ||||
chr1:100132868-100133257 | Common:3; Rare:151 | ||||
chr1:100133277-100133385 | Common:2; Rare:38 | ||||
chr1:100249563-100249638 | Common:1; Rare:15 | ||||
chr1:100249761-100250042 | Common:4; Rare:100; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:100265649-100265839 | Common:2; Rare:33 | ||||
chr1:100266065-100266344 | Common:3; Rare:97 | ||||
chr1:100266690-100266792 | Rare:17 | ||||
chr1:100351272-100351443 | Rare:37 | ||||
chr1:100351549-100351841 | Common:3; Rare:97 | ||||
chr1:100351958-100352023 | Common:5; Rare:20 |