Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:95070842-95071008 | Common:1; Rare:27 | ||||
chr11:95151005-95151212 | Common:2; Rare:55 | ||||
chr11:95163841-95163863 | Rare:3 | ||||
chr11:95203785-95203951 | Rare:25 | ||||
chr11:95820383-95820532 | Rare:22 | ||||
chr11:95820605-95820891 | Common:1; Rare:50 | ||||
chr11:95823058-95823365 | Common:3; Rare:60 | ||||
chr11:95824080-95824503 | Common:5; Rare:90 | ||||
chr11:95826616-95826714 | Common:1; Rare:23 | ||||
chr11:95827546-95827719 | Common:2; Rare:37 | ||||
chr11:95835375-95835504 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
chr11:95845059-95845265 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr11:95847873-95848037 | Common:2; Rare:43 | ||||
chr11:95861994-95862354 | Common:3; Rare:85; Clinvar:4; Clinvar (benign):2 | ||||
chr11:95877004-95877230 | Rare:33 |