Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:121928003-121928047 | Rare:14 | ||||
chr10:122112822-122112994 | Common:3; Rare:58 | ||||
chr10:122374434-122374776 | Common:1; Rare:109 | ||||
chr10:122879531-122879685 | Common:3; Rare:44 | ||||
chr10:122954202-122954499 | Rare:110 | ||||
chr10:123008791-123009023 | Common:5; Rare:63; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124791804-124791938 | Common:1; Rare:66 | ||||
chr10:125719487-125719721 | Rare:71 | ||||
chr10:125823200-125823585 | Common:1; Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896310-125896599 | Common:2; Rare:16 | ||||
chr10:126905302-126905460 | Rare:61 | ||||
chr10:128047432-128047610 | Common:2; Rare:57 | ||||
chr10:129466971-129467280 | Common:3; Rare:121 | ||||
chr10:132331792-132332166 | Common:16; Rare:123 | ||||
chr10:133308835-133308982 | Rare:69 |