Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:78417755-78418029 | Common:1; Rare:111 | ||||
chr11:83071794-83072111 | Common:4; Rare:89 | ||||
chr11:83193651-83193797 | Common:1; Rare:64 | ||||
chr11:83285915-83286130 | Common:3; Rare:102 | ||||
chr11:85628319-85628664 | Common:7; Rare:120 | ||||
chr11:86244979-86245250 | Common:1; Rare:114 | ||||
chr11:87037742-87038040 | Common:3; Rare:139 | ||||
chr11:88337661-88337888 | Common:4; Rare:109; Clinvar:6; Clinvar (benign):3 | ||||
chr11:90223006-90223147 | Common:1; Rare:53 | ||||
chr11:93741478-93741702 | Common:5; Rare:82 | ||||
chr11:93784179-93784374 | Common:3; Rare:60 | ||||
chr11:94493789-94494040 | Common:3; Rare:73; Clinvar (benign):1 | ||||
chr11:94973531-94973711 | Rare:56 | ||||
chr11:95067452-95067569 | Rare:41 | ||||
chr11:95789478-95789853 | Common:3; Rare:174 |