Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:119818610-119818788 | Rare:56 | ||||
chr10:119892518-119892816 | Common:3; Rare:112 | ||||
chr10:120851125-120851406 | Common:7; Rare:87 | ||||
chr10:121927708-121927881 | Common:2; Rare:58 | ||||
chr10:121927890-121928068 | Common:1; Rare:67 | ||||
chr10:121928436-121928548 | Rare:29 | ||||
chr10:122163517-122163836 | Common:2; Rare:84 | ||||
chr10:122374412-122374784 | Common:2; Rare:116 | ||||
chr10:122954168-122954508 | Common:1; Rare:124 | ||||
chr10:122980341-122980482 | Common:1; Rare:38 | ||||
chr10:123008758-123009032 | Common:6; Rare:76; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124418882-124419092 | Common:4; Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
chr10:124461720-124461890 | Common:4; Rare:64 | ||||
chr10:124791701-124791953 | Common:2; Rare:121 | ||||
chr10:124801536-124801878 | Common:1; Rare:103 |