Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:68038915-68039087 | Rare:51; Clinvar:1 | ||||
chr11:68271883-68272223 | Common:2; Rare:144 | ||||
chr11:68460221-68460312 | Common:2; Rare:50 | ||||
chr11:68903806-68903943 | Common:4; Rare:59; Clinvar (benign):6 | ||||
chr11:69013164-69013312 | Common:3; Rare:40 | ||||
chr11:69641428-69641508 | Rare:15 | ||||
chr11:70165176-70165568 | Common:1; Rare:99 | ||||
chr11:70398421-70398596 | Common:2; Rare:63 | ||||
chr11:71448357-71448624 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
chr11:71787305-71787539 | Common:14; Rare:86 | ||||
chr11:72009127-72009333 | Rare:76 | ||||
chr11:72041062-72041410 | Common:1; Rare:57 | ||||
chr11:72041949-72042238 | Common:1; Rare:61 | ||||
chr11:72080190-72080341 | Common:6; Rare:21 | ||||
chr11:72080471-72080845 | Common:1; Rare:84; Clinvar:6 |