Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:34916311-34916669 | Common:10; Rare:147; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr11:35139018-35139181 | Common:1; Rare:35 | ||||
chr11:35525596-35525816 | Rare:49 | ||||
chr11:36510240-36510382 | Rare:43 | ||||
chr11:43358831-43358979 | Rare:73 | ||||
chr11:45847221-45847487 | Common:2; Rare:108 | ||||
chr11:46846218-46846412 | Common:1; Rare:53 | ||||
chr11:47186408-47186529 | Rare:33 | ||||
chr11:47270018-47270161 | Common:1; Rare:52 | ||||
chr11:47565513-47565620 | Common:2; Rare:19 | ||||
chr11:47578968-47579085 | Rare:60; Clinvar:2 | ||||
chr11:47642467-47642815 | Rare:129 | ||||
chr11:47848325-47848398 | Rare:35 | ||||
chr11:57311454-57311724 | Common:1; Rare:69 | ||||
chr11:57324890-57325143 | Common:1; Rare:76 |