Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122954186-122954508 | Common:1; Rare:119 | ||||
chr10:122980350-122980431 | Common:1; Rare:11 | ||||
chr10:123008791-123009041 | Common:5; Rare:74; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124418875-124419103 | Common:5; Rare:106; Clinvar:4; Clinvar (benign):1 | ||||
chr10:124791809-124791938 | Common:1; Rare:64 | ||||
chr10:125719462-125719757 | Common:1; Rare:104 | ||||
chr10:125823200-125823594 | Common:1; Rare:139; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125896456-125896628 | Common:4; Rare:18 | ||||
chr10:126905297-126905465 | Rare:64 | ||||
chr10:127906940-127907137 | Common:2; Rare:58 | ||||
chr10:128047421-128047635 | Common:2; Rare:69 | ||||
chr10:130136321-130136487 | Common:7; Rare:66 | ||||
chr10:131981865-131982154 | Common:4; Rare:107 | ||||
chr10:132331818-132332199 | Common:13; Rare:117 | ||||
chr10:133308818-133308989 | Rare:81 |