Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:125719456-125719726 | Rare:85 | ||||
chr10:125725423-125725701 | Rare:59 | ||||
chr10:125823031-125823721 | Common:3; Rare:234; Clinvar:2; Clinvar (benign):3 | ||||
chr10:125896485-125896630 | Common:3; Rare:18 | ||||
chr10:126905293-126905466 | Rare:65 | ||||
chr10:127906818-127907277 | Common:4; Rare:118 | ||||
chr10:127986908-127987204 | Common:3; Rare:65 | ||||
chr10:131981889-131982154 | Common:2; Rare:98 | ||||
chr10:132307880-132308142 | Common:4; Rare:80 | ||||
chr10:132331813-132332122 | Common:12; Rare:100 | ||||
chr10:133308823-133309095 | Common:2; Rare:111 | ||||
chr10:133309876-133310292 | Rare:130 | ||||
chr11:207339-207733 | Common:8; Rare:135 | ||||
chr11:208615-208882 | Rare:96 | ||||
chr11:236191-236491 | Common:7; Rare:109 |