Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11012971-11013092 | Rare:43 | ||||
chr1:11013017-11013308 | Common:1; Rare:141 | ||||
chr1:11059915-11060409 | Common:8; Rare:387 | ||||
chr1:11099339-11099480 | Rare:63 | ||||
chr1:11099749-11100062 | Common:9; Rare:272 | ||||
chr1:11262443-11262945 | Common:8; Rare:373 | ||||
chr1:11272875-11273306 | Common:3; Rare:333; Clinvar:3; Clinvar (benign):3 | ||||
chr1:11273424-11273571 | Common:3; Rare:125; Clinvar:4; Clinvar (benign):3 | ||||
chr1:11479138-11479242 | Common:4; Rare:44 | ||||
chr1:11654687-11654939 | Common:9; Rare:145 | ||||
chr1:11690620-11691010 | Common:2; Rare:78 | ||||
chr1:11690986-11691830 | Common:11; Rare:225 | ||||
chr1:11735938-11736319 | Common:9; Rare:215 | ||||
chr1:11736350-11736770 | Common:1; Rare:93 | ||||
chr1:11805438-11805683 | Common:4; Rare:81 |