| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69675303-69675454 | Rare:41 | ||||
| chr11:71448344-71448739 | Common:5; Rare:104; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71452970-71453241 | Common:4; Rare:70 | ||||
| chr11:71928398-71928465 | Rare:20 | ||||
| chr11:71928887-71929061 | Common:1; Rare:58 | ||||
| chr11:72080449-72080830 | Common:2; Rare:86; Clinvar:7 | ||||
| chr11:72103250-72103518 | Rare:74 | ||||
| chr11:72112256-72112515 | Rare:64 | ||||
| chr11:72112639-72112859 | Common:2; Rare:98 | ||||
| chr11:72722270-72722413 | Rare:28 | ||||
| chr11:72752396-72752583 | Common:2; Rare:54 | ||||
| chr11:72814054-72814455 | Common:4; Rare:119 | ||||
| chr11:73141357-73141493 | Rare:38 | ||||
| chr11:73141709-73141780 | Rare:22 | ||||
| chr11:73598071-73598281 | Common:1; Rare:57 |