Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:57567612-57567968 | Common:2; Rare:95 | ||||
chr11:57597580-57597711 | Rare:30; Clinvar:3; Clinvar (benign):1 | ||||
chr11:57712175-57712630 | Common:9; Rare:153 | ||||
chr11:57761691-57761942 | Rare:45 | ||||
chr11:58905324-58905389 | Common:1; Rare:9 | ||||
chr11:59107021-59107243 | Common:2; Rare:64 | ||||
chr11:59142694-59142939 | Common:1; Rare:44 | ||||
chr11:60906514-60906823 | Rare:76 | ||||
chr11:60914057-60914238 | Common:1; Rare:52 | ||||
chr11:61333038-61333266 | Rare:80 | ||||
chr11:61361870-61362023 | Common:1; Rare:35 | ||||
chr11:61362278-61362420 | Common:1; Rare:41; Clinvar:6 | ||||
chr11:61429920-61430144 | Common:1; Rare:101; Clinvar (benign):2 | ||||
chr11:61792564-61792955 | Common:5; Rare:108 | ||||
chr11:61816133-61816327 | Rare:53 |