Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:119080772-119080929 | Rare:64 | ||||
chr10:119178786-119178940 | Common:3; Rare:60 | ||||
chr10:119542630-119542899 | Common:4; Rare:80 | ||||
chr10:119596943-119597248 | Common:1; Rare:85 | ||||
chr10:119651234-119651386 | Common:4; Rare:58; Clinvar (benign):2 | ||||
chr10:119892561-119892769 | Common:2; Rare:80 | ||||
chr10:121927976-121928068 | Rare:31 | ||||
chr10:122374422-122374784 | Common:2; Rare:114 | ||||
chr10:122879531-122879714 | Common:3; Rare:48 | ||||
chr10:122954197-122954496 | Rare:109 | ||||
chr10:123008788-123009028 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124418881-124419086 | Common:4; Rare:94; Clinvar:3; Clinvar (benign):1 | ||||
chr10:124461733-124461899 | Common:4; Rare:64 | ||||
chr10:124791823-124791948 | Rare:57 | ||||
chr10:125719453-125719761 | Common:1; Rare:109 |