Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:69641232-69641508 | Rare:78 | ||||
chr11:69675294-69675491 | Rare:56 | ||||
chr11:70203133-70203346 | Common:3; Rare:82 | ||||
chr11:70398421-70398623 | Common:2; Rare:74 | ||||
chr11:71448275-71448749 | Common:5; Rare:128; Clinvar:4; Clinvar (benign):1 | ||||
chr11:71928937-71929067 | Common:1; Rare:44 | ||||
chr11:72008965-72009389 | Common:1; Rare:133 | ||||
chr11:72041486-72041722 | Rare:36 | ||||
chr11:72041840-72041905 | Common:2; Rare:10 | ||||
chr11:72080232-72080341 | Common:6; Rare:15 | ||||
chr11:72080390-72080646 | Common:1; Rare:62; Clinvar:4 | ||||
chr11:72080685-72080835 | Rare:35; Clinvar:2 | ||||
chr11:72112233-72112307 | Rare:14 | ||||
chr11:72112656-72112864 | Common:3; Rare:90 | ||||
chr11:72223798-72223932 | Rare:38 |