Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:69048808-69048953 | Common:2; Rare:52 | ||||
chr11:69640958-69641259 | Common:1; Rare:63 | ||||
chr11:69675309-69675488 | Rare:50 | ||||
chr11:70203113-70203330 | Common:4; Rare:84 | ||||
chr11:70398421-70398596 | Common:2; Rare:63 | ||||
chr11:71448347-71448690 | Common:4; Rare:91; Clinvar:3; Clinvar (benign):1 | ||||
chr11:71787312-71787546 | Common:14; Rare:91 | ||||
chr11:71928930-71929064 | Common:1; Rare:45 | ||||
chr11:72039751-72040063 | Common:1; Rare:54 | ||||
chr11:72041843-72041894 | Common:1; Rare:9 | ||||
chr11:72080238-72080341 | Common:6; Rare:15 | ||||
chr11:72080420-72080652 | Common:1; Rare:56; Clinvar:4 | ||||
chr11:72080685-72080853 | Rare:38; Clinvar:2 | ||||
chr11:72223786-72223894 | Rare:31 | ||||
chr11:72752396-72752584 | Common:2; Rare:55 |