Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:68903770-68903947 | Common:4; Rare:84; Clinvar (benign):6 | ||||
chr11:69299042-69299270 | Common:2; Rare:47 | ||||
chr11:69640945-69641250 | Common:1; Rare:62 | ||||
chr11:69675303-69675503 | Rare:54 | ||||
chr11:70398353-70398614 | Common:2; Rare:95 | ||||
chr11:71448321-71448707 | Common:4; Rare:103; Clinvar:3; Clinvar (benign):1 | ||||
chr11:71453005-71453284 | Common:1; Rare:78 | ||||
chr11:71928915-71929089 | Common:1; Rare:54 | ||||
chr11:72041062-72041331 | Common:1; Rare:49 | ||||
chr11:72080449-72080861 | Common:2; Rare:91; Clinvar:7 | ||||
chr11:72103187-72103498 | Rare:87 | ||||
chr11:72112223-72112508 | Rare:73 | ||||
chr11:72112653-72112958 | Common:4; Rare:130 | ||||
chr11:72752347-72752529 | Common:2; Rare:59 | ||||
chr11:72814043-72814446 | Common:4; Rare:121 |