Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:119067626-119067821 | Common:3; Rare:65 | ||||
chr11:119121284-119121621 | Common:1; Rare:75 | ||||
chr11:119206178-119206369 | Common:5; Rare:87; Clinvar:7; Clinvar (benign):4 | ||||
chr11:121292614-121292798 | Rare:62; Clinvar:3 | ||||
chr11:123062062-123062311 | Common:5; Rare:103 | ||||
chr11:123062387-123062666 | Common:4; Rare:131 | ||||
chr11:124673710-124673934 | Common:4; Rare:68 | ||||
chr11:124953954-124954203 | Common:5; Rare:75 | ||||
chr11:125592451-125592933 | Common:6; Rare:164 | ||||
chr11:125625874-125626003 | Rare:43 | ||||
chr11:125887480-125887727 | Common:2; Rare:78 | ||||
chr11:125903165-125903327 | Rare:39 | ||||
chr11:126211620-126211819 | Rare:91 | ||||
chr11:126268814-126269207 | Common:2; Rare:152; Clinvar:2; Clinvar (benign):4 | ||||
chr11:126283002-126283134 | Common:1; Rare:51 |