Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:763267-763389 | Common:9; Rare:75; Clinvar:2 | ||||
chr11:783517-783674 | Rare:48 | ||||
chr11:812676-812877 | Rare:70 | ||||
chr11:819718-820150 | Common:3; Rare:117; Clinvar:2; Clinvar (benign):3 | ||||
chr11:840454-840498 | Common:2; Rare:12 | ||||
chr11:880904-880954 | Rare:7 | ||||
chr11:927417-927588 | Common:5; Rare:41 | ||||
chr11:973546-973707 | Common:1; Rare:35 | ||||
chr11:1478075-1478249 | Common:2; Rare:42 | ||||
chr11:1792905-1792916 | |||||
chr11:1908680-1908831 | Rare:31 | ||||
chr11:2138328-2138392 | Common:1; Rare:21 | ||||
chr11:2377997-2378110 | Common:2; Rare:31 | ||||
chr11:2383066-2383233 | Common:1; Rare:43 | ||||
chr11:2648083-2648110 | Rare:2 |