| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69048728-69048970 | Common:5; Rare:84 | ||||
| chr11:69640986-69641080 | Rare:26 | ||||
| chr11:69641085-69641510 | Common:1; Rare:104 | ||||
| chr11:69673627-69673651 | Rare:8 | ||||
| chr11:69675204-69675519 | Common:1; Rare:98 | ||||
| chr11:70077911-70078084 | Common:1; Rare:43 | ||||
| chr11:70203027-70203423 | Common:5; Rare:144 | ||||
| chr11:70270463-70270763 | Common:2; Rare:121 | ||||
| chr11:70371350-70371610 | Common:7; Rare:26 | ||||
| chr11:70398362-70398866 | Common:2; Rare:147 | ||||
| chr11:70422052-70422488 | Common:3; Rare:79 | ||||
| chr11:71448272-71448601 | Common:3; Rare:94; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:71480073-71480175 | Rare:14 | ||||
| chr11:71787350-71787602 | Common:13; Rare:116 | ||||
| chr11:71928395-71929106 | Common:1; Rare:199 |