Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882482-179882928 | Rare:219; Clinvar:9; Clinvar (benign):2 | ||||
chr1:179954500-179954814 | Common:2; Rare:76 | ||||
chr1:181088758-181088960 | Common:1; Rare:72 | ||||
chr1:182604346-182604553 | Rare:52 | ||||
chr1:182789678-182789778 | Common:1; Rare:31 | ||||
chr1:182839202-182839358 | Common:1; Rare:62 | ||||
chr1:182858639-182858819 | Common:2; Rare:45 | ||||
chr1:183472172-183472513 | Common:3; Rare:106 | ||||
chr1:183635686-183635863 | Common:1; Rare:56 | ||||
chr1:184051483-184051756 | Common:3; Rare:77 | ||||
chr1:185045241-185045599 | Common:2; Rare:125 | ||||
chr1:185156892-185157272 | Common:2; Rare:105 | ||||
chr1:186375446-186375892 | Common:1; Rare:123 | ||||
chr1:192575496-192575810 | Common:3; Rare:64 | ||||
chr1:192808617-192809078 | Common:5; Rare:160 |