Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:560720-561003 | Common:5; Rare:128 | ||||
chr11:576418-576531 | Rare:45 | ||||
chr11:695731-695826 | Rare:32 | ||||
chr11:747306-747493 | Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777451-777588 | Common:1; Rare:61 | ||||
chr11:809498-809773 | Common:3; Rare:81 | ||||
chr11:809843-810037 | Common:2; Rare:90 | ||||
chr11:827218-827322 | Common:2; Rare:24 | ||||
chr11:832849-833021 | Common:7; Rare:62 | ||||
chr11:842446-842978 | Common:8; Rare:220 | ||||
chr11:843964-844154 | Common:1; Rare:46 | ||||
chr11:1309588-1309748 | Common:1; Rare:75 | ||||
chr11:1868554-1868833 | Rare:58 | ||||
chr11:1919457-1919754 | Rare:76; Clinvar:2; Clinvar (benign):1 | ||||
chr11:1921305-1921399 | Common:2; Rare:19 |