Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:6390241-6390503 | Common:2; Rare:75 | ||||
chr11:6473871-6474107 | Rare:77 | ||||
chr11:6481276-6481559 | Common:5; Rare:127 | ||||
chr11:6603454-6603887 | Common:4; Rare:133; Clinvar (benign):3 | ||||
chr11:6604059-6604358 | Common:1; Rare:84; Clinvar (benign):3 | ||||
chr11:6604608-6604836 | Common:3; Rare:60 | ||||
chr11:6614971-6615122 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
chr11:6683234-6683430 | Common:3; Rare:95 | ||||
chr11:6926288-6926597 | Common:5; Rare:91 | ||||
chr11:6926846-6926941 | Common:1; Rare:22 | ||||
chr11:7020323-7020489 | Rare:59 | ||||
chr11:7485223-7485545 | Common:1; Rare:59 | ||||
chr11:7513612-7514081 | Common:6; Rare:139 | ||||
chr11:8682628-8682826 | Common:2; Rare:86 | ||||
chr11:8910932-8911358 | Common:7; Rare:118 |