Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:156054609-156054892 | Common:3; Rare:82 | ||||
chr1:156054921-156055105 | Common:1; Rare:43 | ||||
chr1:156081262-156081342 | Rare:16 | ||||
chr1:156082441-156082706 | Rare:62 | ||||
chr1:156114529-156114839 | Common:1; Rare:67; Clinvar:4; Clinvar (benign):2 | ||||
chr1:156134401-156134988 | Common:2; Rare:139; Clinvar:22; Clinvar (benign):13; Clinvar (pathogenic):14 | ||||
chr1:156135961-156136437 | Common:4; Rare:151; Clinvar:32; Clinvar (benign):21; Clinvar (pathogenic):12 | ||||
chr1:156193832-156194149 | Common:3; Rare:83 | ||||
chr1:156212882-156213166 | Common:1; Rare:102 | ||||
chr1:156282460-156282566 | Common:1; Rare:20 | ||||
chr1:156282743-156282941 | Common:2; Rare:64 | ||||
chr1:156338142-156338542 | Common:2; Rare:145 | ||||
chr1:156500736-156501015 | Common:1; Rare:102 | ||||
chr1:156598313-156598370 | Rare:20 | ||||
chr1:156601407-156601754 | Common:3; Rare:100 |