Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122954186-122954452 | Rare:96 | ||||
chr10:123008773-123009026 | Common:6; Rare:67; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124791823-124791976 | Rare:74 | ||||
chr10:125719453-125719716 | Rare:81 | ||||
chr10:125823184-125823596 | Common:2; Rare:147; Clinvar:1; Clinvar (benign):2 | ||||
chr10:126905133-126905460 | Common:2; Rare:116 | ||||
chr10:128047463-128047661 | Common:4; Rare:64 | ||||
chr10:130136325-130136420 | Common:4; Rare:34 | ||||
chr10:132307895-132308167 | Common:5; Rare:81 | ||||
chr10:132331795-132332113 | Common:14; Rare:107 | ||||
chr10:133308834-133308952 | Rare:52 | ||||
chr10:133373348-133373677 | Common:2; Rare:121; Clinvar (benign):1 | ||||
chr11:207332-207732 | Common:8; Rare:135 | ||||
chr11:208617-208847 | Rare:81 | ||||
chr11:236726-237010 | Common:3; Rare:82 |