Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173477027-173477490 | Common:5; Rare:159 | ||||
chr1:173824384-173824722 | Rare:61; Clinvar:2 | ||||
chr1:173867986-173868199 | Common:1; Rare:72 | ||||
chr1:179081984-179082098 | Common:1; Rare:37 | ||||
chr1:179882070-179882306 | Common:1; Rare:54 | ||||
chr1:179882482-179882853 | Rare:175; Clinvar:7; Clinvar (benign):2 | ||||
chr1:182391327-182391438 | Rare:23 | ||||
chr1:182839181-182839391 | Common:1; Rare:93 | ||||
chr1:183635643-183636109 | Common:5; Rare:130 | ||||
chr1:185156927-185157175 | Rare:58 | ||||
chr1:186375226-186375451 | Rare:44 | ||||
chr1:186375693-186375923 | Common:1; Rare:61 | ||||
chr1:186680400-186680735 | Common:3; Rare:77 | ||||
chr1:193059314-193059665 | Rare:160 | ||||
chr1:202927198-202927328 | Common:4; Rare:61 |