| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70398349-70398614 | Common:2; Rare:96 | ||||
| chr11:70826507-70826590 | Rare:27 | ||||
| chr11:71448336-71448708 | Common:4; Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452987-71453290 | Common:3; Rare:86 | ||||
| chr11:71787312-71787567 | Common:15; Rare:105 | ||||
| chr11:71928634-71929089 | Common:1; Rare:124 | ||||
| chr11:71998853-71998981 | Rare:30 | ||||
| chr11:72009159-72009278 | Rare:52 | ||||
| chr11:72039780-72039929 | Common:1; Rare:22 | ||||
| chr11:72040685-72040891 | Rare:42 | ||||
| chr11:72041008-72041373 | Common:1; Rare:68 | ||||
| chr11:72041528-72041759 | Rare:40 | ||||
| chr11:72041832-72042036 | Common:2; Rare:37 | ||||
| chr11:72080232-72080341 | Common:6; Rare:15 | ||||
| chr11:72080366-72080867 | Common:2; Rare:119; Clinvar:10 |