Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882234-179882311 | Rare:14 | ||||
chr1:179882493-179882860 | Rare:176; Clinvar:7; Clinvar (benign):2 | ||||
chr1:180502270-180502673 | Common:1; Rare:142 | ||||
chr1:180631821-180632049 | Common:4; Rare:72 | ||||
chr1:181088494-181088704 | Rare:67 | ||||
chr1:182789604-182789778 | Common:2; Rare:53 | ||||
chr1:183186131-183186378 | Common:4; Rare:60; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:183635666-183636094 | Common:4; Rare:123 | ||||
chr1:184051564-184051768 | Common:3; Rare:71 | ||||
chr1:184754812-184755146 | Common:1; Rare:79 | ||||
chr1:185156915-185157164 | Rare:61 | ||||
chr1:185317190-185317468 | Common:1; Rare:82 | ||||
chr1:186375094-186375548 | Rare:124 | ||||
chr1:186375609-186375923 | Common:1; Rare:90 | ||||
chr1:186680265-186680688 | Common:3; Rare:98 |