Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:118252239-118252377 | Rare:49 | ||||
chr11:118264242-118264648 | Common:1; Rare:59 | ||||
chr11:118344268-118344414 | Common:1; Rare:26; Clinvar:1; Clinvar (benign):1 | ||||
chr11:118607426-118607638 | Common:1; Rare:31 | ||||
chr11:118621314-118621391 | Rare:15 | ||||
chr11:118790904-118791255 | Rare:100 | ||||
chr11:118910510-118910683 | Common:1; Rare:59 | ||||
chr11:118997980-118998193 | Common:4; Rare:66 | ||||
chr11:119018280-119018795 | Common:13; Rare:199 | ||||
chr11:119057127-119057437 | Common:3; Rare:122 | ||||
chr11:119067730-119067826 | Rare:35 | ||||
chr11:119149173-119149269 | Rare:23 | ||||
chr11:119206186-119206391 | Common:5; Rare:90; Clinvar:8; Clinvar (benign):4 | ||||
chr11:119311348-119311544 | Rare:74 | ||||
chr11:119317103-119317275 | Rare:58 |