Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:33736392-33736605 | Common:2; Rare:66 | ||||
chr11:34916287-34916676 | Common:10; Rare:158; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr11:35138949-35139202 | Common:1; Rare:55 | ||||
chr11:35943936-35944111 | Common:3; Rare:59 | ||||
chr11:43358814-43358953 | Rare:61 | ||||
chr11:45917865-45918146 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
chr11:46846224-46846412 | Common:1; Rare:51 | ||||
chr11:47186408-47186528 | Rare:33 | ||||
chr11:47269981-47270166 | Common:1; Rare:61 | ||||
chr11:47565534-47565625 | Common:2; Rare:14 | ||||
chr11:47578960-47579085 | Rare:65; Clinvar:2 | ||||
chr11:57712184-57712618 | Common:9; Rare:144 | ||||
chr11:59142764-59142860 | Rare:16 | ||||
chr11:60906507-60906881 | Rare:91 | ||||
chr11:61333065-61333275 | Common:1; Rare:76 |