Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110007684-110008101 | Common:1; Rare:120 | ||||
chr10:110919278-110919629 | Common:7; Rare:92 | ||||
chr10:112183717-112183821 | Common:2; Rare:39 | ||||
chr10:112446899-112447282 | Common:3; Rare:93 | ||||
chr10:113854369-113854867 | Common:1; Rare:112 | ||||
chr10:118754999-118755319 | Common:1; Rare:102 | ||||
chr10:119080772-119080923 | Rare:59 | ||||
chr10:119178786-119178940 | Common:3; Rare:60 | ||||
chr10:119892536-119892777 | Common:3; Rare:91 | ||||
chr10:121928006-121928068 | Rare:14 | ||||
chr10:122879518-122879735 | Common:4; Rare:57 | ||||
chr10:122954174-122954508 | Common:1; Rare:120 | ||||
chr10:123008782-123009011 | Common:5; Rare:62; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124791765-124791986 | Common:1; Rare:118 | ||||
chr10:125719453-125719761 | Common:1; Rare:109 |