Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:118565899-118566195 | Common:1; Rare:66 | ||||
chr11:118790885-118791263 | Rare:112 | ||||
chr11:118997980-118998200 | Common:4; Rare:68 | ||||
chr11:119018280-119018452 | Common:6; Rare:71 | ||||
chr11:119018622-119018795 | Common:5; Rare:71 | ||||
chr11:119057110-119057437 | Common:3; Rare:126 | ||||
chr11:119067639-119067826 | Common:3; Rare:63 | ||||
chr11:119121307-119121631 | Common:1; Rare:70 | ||||
chr11:119206180-119206390 | Common:5; Rare:95; Clinvar:8; Clinvar (benign):4 | ||||
chr11:119317097-119317275 | Rare:59 | ||||
chr11:120128841-120129069 | Common:1; Rare:46 | ||||
chr11:120336145-120336449 | Rare:128 | ||||
chr11:121292569-121292801 | Rare:82; Clinvar:3 | ||||
chr11:123062062-123062311 | Common:5; Rare:103 | ||||
chr11:123062428-123062663 | Common:3; Rare:108 |