Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:96341778-96341887 | Rare:35 | ||||
chr11:102272645-102272860 | Common:4; Rare:33 | ||||
chr11:110430618-110430667 | Rare:7 | ||||
chr11:112152064-112152318 | Common:1; Rare:37 | ||||
chr11:114073643-114073884 | Rare:40 | ||||
chr11:116814048-116814207 | Common:2; Rare:26 | ||||
chr11:116835659-116835790 | Rare:36; Clinvar (benign):1 | ||||
chr11:116874351-116874647 | Common:1; Rare:53 | ||||
chr11:117195302-117195408 | Rare:11 | ||||
chr11:117195574-117195841 | Common:1; Rare:50 | ||||
chr11:118406774-118406949 | Common:2; Rare:34 | ||||
chr11:118533988-118534308 | Common:2; Rare:91 | ||||
chr11:118534324-118534547 | Common:1; Rare:70 | ||||
chr11:118922251-118922263 | Rare:3 | ||||
chr11:119013155-119013260 | Common:1; Rare:39 |