Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:2902050-2902355 | Common:1; Rare:68 | ||||
chr11:3797491-3797721 | Rare:86 | ||||
chr11:3855555-3855754 | Common:2; Rare:41 | ||||
chr11:4094749-4094877 | Rare:38 | ||||
chr11:4393651-4393820 | Rare:42 | ||||
chr11:4608131-4608405 | Common:1; Rare:83 | ||||
chr11:5624893-5625033 | Rare:22 | ||||
chr11:6320495-6320597 | Common:2; Rare:31 | ||||
chr11:6390237-6390502 | Common:2; Rare:76 | ||||
chr11:6481276-6481569 | Common:5; Rare:131 | ||||
chr11:6603542-6603822 | Common:4; Rare:86; Clinvar (benign):3 | ||||
chr11:6683234-6683644 | Common:6; Rare:157 | ||||
chr11:7513616-7514050 | Common:6; Rare:130 | ||||
chr11:7577424-7577545 | Rare:25 | ||||
chr11:7673448-7673574 | Common:1; Rare:43 |