Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:119892548-119892785 | Common:3; Rare:90 | ||||
chr10:120851281-120851487 | Common:2; Rare:86 | ||||
chr10:121927953-121928103 | Common:1; Rare:53 | ||||
chr10:121928429-121928522 | Rare:27 | ||||
chr10:122879531-122879698 | Common:3; Rare:46 | ||||
chr10:122954185-122954506 | Common:1; Rare:118 | ||||
chr10:122980366-122980431 | Common:1; Rare:10 | ||||
chr10:123008785-123009023 | Common:5; Rare:65; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124092336-124092539 | Rare:52 | ||||
chr10:124092724-124092839 | Rare:30 | ||||
chr10:124093027-124093350 | Common:4; Rare:78 | ||||
chr10:124093497-124093681 | Common:2; Rare:32 | ||||
chr10:124093688-124093899 | Common:1; Rare:41 | ||||
chr10:124418882-124419160 | Common:6; Rare:125; Clinvar:3; Clinvar (benign):1 | ||||
chr10:124461733-124461871 | Common:4; Rare:53 |