Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:236867-237144 | Common:3; Rare:109 | ||||
chr11:289005-289198 | Common:1; Rare:55 | ||||
chr11:308053-308319 | Common:7; Rare:86 | ||||
chr11:320689-320936 | Common:5; Rare:96; Clinvar:1 | ||||
chr11:450152-450458 | Rare:90 | ||||
chr11:498495-498811 | Rare:120 | ||||
chr11:506610-507021 | Common:3; Rare:125 | ||||
chr11:507118-507297 | Rare:60 | ||||
chr11:535422-535751 | Common:5; Rare:139; Clinvar (benign):1 | ||||
chr11:560691-561024 | Common:6; Rare:155 | ||||
chr11:576411-576582 | Rare:72 | ||||
chr11:615936-616104 | Common:1; Rare:50 | ||||
chr11:695034-695371 | Common:1; Rare:78 | ||||
chr11:695613-695833 | Rare:55 | ||||
chr11:777449-777621 | Common:1; Rare:77 |