Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:18634278-18634593 | Common:3; Rare:112 | ||||
chr11:27506730-27506855 | Common:1; Rare:58 | ||||
chr11:30322973-30323162 | Common:1; Rare:55 | ||||
chr11:31369737-31369888 | Rare:47 | ||||
chr11:31509589-31509820 | Common:1; Rare:80 | ||||
chr11:33161453-33161651 | Common:6; Rare:51 | ||||
chr11:34916302-34916578 | Common:8; Rare:116; Clinvar:3; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr11:35663100-35663418 | Rare:113 | ||||
chr11:36510253-36510353 | Rare:28 | ||||
chr11:43880692-43880863 | Common:1; Rare:37 | ||||
chr11:46277970-46278209 | Rare:63 | ||||
chr11:46377814-46377914 | Rare:15 | ||||
chr11:46700567-46700818 | Common:1; Rare:64 | ||||
chr11:46846258-46846422 | Common:1; Rare:48 | ||||
chr11:47248796-47248957 | Rare:66 |