Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:576418-576582 | Rare:68 | ||||
chr11:695731-695818 | Rare:29 | ||||
chr11:777458-777598 | Common:1; Rare:61 | ||||
chr11:809521-810038 | Common:5; Rare:193 | ||||
chr11:842487-842974 | Common:8; Rare:201 | ||||
chr11:844014-844163 | Common:1; Rare:34 | ||||
chr11:1309560-1309778 | Common:2; Rare:96 | ||||
chr11:1919622-1919748 | Rare:32; Clinvar (benign):1 | ||||
chr11:2301889-2302136 | Common:2; Rare:64 | ||||
chr11:2302915-2303179 | Common:1; Rare:66 | ||||
chr11:2461160-2461487 | Common:1; Rare:87 | ||||
chr11:3379089-3379353 | Common:4; Rare:69 | ||||
chr11:3855555-3855711 | Common:2; Rare:32 | ||||
chr11:4094749-4094867 | Rare:36 | ||||
chr11:5624897-5625033 | Rare:20 |