Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122954197-122954496 | Rare:109 | ||||
chr10:123008788-123009023 | Common:5; Rare:63; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124092369-124092623 | Common:1; Rare:63 | ||||
chr10:124418892-124419092 | Common:4; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
chr10:124791790-124791930 | Common:1; Rare:77 | ||||
chr10:124801706-124801847 | Rare:47 | ||||
chr10:125719453-125719761 | Common:1; Rare:109 | ||||
chr10:125823200-125823568 | Common:1; Rare:121; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896307-125896618 | Common:5; Rare:25 | ||||
chr10:126905124-126905465 | Common:2; Rare:120 | ||||
chr10:130136327-130136498 | Common:7; Rare:67 | ||||
chr10:132331806-132332164 | Common:15; Rare:115 | ||||
chr10:133308835-133308997 | Rare:76 | ||||
chr11:207331-207746 | Common:9; Rare:141 | ||||
chr11:208615-208865 | Rare:91 |