Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:118264284-118264586 | Common:1; Rare:50 | ||||
chr11:118401284-118401710 | Rare:145 | ||||
chr11:118790894-118791290 | Rare:126 | ||||
chr11:118997980-118998246 | Common:4; Rare:91 | ||||
chr11:119018280-119018457 | Common:6; Rare:72 | ||||
chr11:119018648-119018795 | Common:5; Rare:66 | ||||
chr11:119057053-119057460 | Common:3; Rare:155 | ||||
chr11:119067630-119067821 | Common:3; Rare:65 | ||||
chr11:119121268-119121627 | Common:1; Rare:85 | ||||
chr11:119206185-119206373 | Common:5; Rare:82; Clinvar:7; Clinvar (benign):4 | ||||
chr11:119317097-119317275 | Rare:59 | ||||
chr11:119381602-119381762 | Common:1; Rare:37 | ||||
chr11:120128442-120128609 | Common:2; Rare:55 | ||||
chr11:121292456-121292786 | Rare:93; Clinvar:3 | ||||
chr11:122882750-122882950 | Rare:56 |