| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67443402-67443625 | Common:2; Rare:84 | ||||
| chr11:67482743-67483154 | Common:2; Rare:92; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:68030367-68030744 | Common:3; Rare:107; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038904-68039079 | Rare:55; Clinvar:1 | ||||
| chr11:68271895-68272102 | Common:2; Rare:89 | ||||
| chr11:68903778-68903943 | Common:4; Rare:79; Clinvar (benign):6 | ||||
| chr11:69293963-69294176 | Common:3; Rare:26 | ||||
| chr11:69640945-69641266 | Common:1; Rare:70 | ||||
| chr11:69675291-69675534 | Common:1; Rare:67 | ||||
| chr11:70398421-70398614 | Common:2; Rare:73 | ||||
| chr11:71448321-71448686 | Common:4; Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928915-71929067 | Common:1; Rare:49 | ||||
| chr11:72080420-72080835 | Common:2; Rare:102; Clinvar:8 | ||||
| chr11:72103183-72103628 | Rare:118 | ||||
| chr11:72722250-72722648 | Rare:86 |