Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:34916258-34916446 | Common:4; Rare:72; Clinvar:3; Clinvar (benign):4 | ||||
chr11:35663107-35663454 | Rare:127 | ||||
chr11:36377349-36377531 | Common:1; Rare:44 | ||||
chr11:36510240-36510353 | Rare:32 | ||||
chr11:43358648-43359096 | Rare:154 | ||||
chr11:44065997-44066371 | Common:3; Rare:95 | ||||
chr11:44066421-44066524 | Common:1; Rare:29 | ||||
chr11:44565563-44565734 | Common:1; Rare:47 | ||||
chr11:45146585-45146658 | Rare:10 | ||||
chr11:45847249-45847483 | Common:2; Rare:91 | ||||
chr11:45917813-45918168 | Common:1; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
chr11:46119444-46119598 | Common:1; Rare:35 | ||||
chr11:46345361-46345525 | Common:1; Rare:59 | ||||
chr11:46380544-46380893 | Common:1; Rare:100 | ||||
chr11:46594008-46594207 | Common:1; Rare:36 |