Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:58573859-58574109 | Common:1; Rare:46 | ||||
chr11:58647095-58647495 | Common:3; Rare:71 | ||||
chr11:59054338-59054416 | Rare:19 | ||||
chr11:59058643-59058919 | Rare:79 | ||||
chr11:59098039-59098222 | Common:1; Rare:36 | ||||
chr11:59102283-59102488 | Common:4; Rare:54 | ||||
chr11:59102507-59102720 | Rare:51 | ||||
chr11:59107973-59108043 | Rare:8 | ||||
chr11:59108202-59108379 | Common:3; Rare:39 | ||||
chr11:59151931-59152011 | Common:1; Rare:25; Clinvar (benign):1 | ||||
chr11:59173948-59174130 | Common:2; Rare:36 | ||||
chr11:59208224-59208371 | Common:2; Rare:21 | ||||
chr11:59209196-59209473 | Common:1; Rare:33 | ||||
chr11:59210443-59210717 | Rare:47 | ||||
chr11:59210733-59211166 | Common:1; Rare:148 |