Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:506756-506966 | Common:2; Rare:71 | ||||
chr11:576412-576519 | Rare:43 | ||||
chr11:777474-777607 | Rare:58 | ||||
chr11:809809-810031 | Common:2; Rare:102 | ||||
chr11:832826-833014 | Common:7; Rare:62 | ||||
chr11:842497-842895 | Common:7; Rare:163 | ||||
chr11:3379089-3379345 | Common:4; Rare:68 | ||||
chr11:4094549-4094897 | Common:2; Rare:97 | ||||
chr11:6390241-6390474 | Common:2; Rare:66 | ||||
chr11:6473884-6474100 | Rare:70 | ||||
chr11:6481299-6481524 | Common:4; Rare:89 | ||||
chr11:6603542-6603822 | Common:4; Rare:86; Clinvar (benign):3 | ||||
chr11:7020318-7020502 | Rare:66 | ||||
chr11:8169019-8169027 | Rare:2 | ||||
chr11:8682628-8682840 | Common:2; Rare:96 |