| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69013107-69013482 | Common:4; Rare:118 | ||||
| chr11:69048703-69048996 | Common:6; Rare:107 | ||||
| chr11:69640983-69641235 | Common:1; Rare:53 | ||||
| chr11:69675308-69675484 | Rare:49 | ||||
| chr11:70077994-70078056 | Common:1; Rare:8 | ||||
| chr11:70203133-70203366 | Common:3; Rare:87 | ||||
| chr11:70398358-70398596 | Common:2; Rare:83 | ||||
| chr11:70826507-70826587 | Rare:26 | ||||
| chr11:71448352-71448690 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:71787312-71787548 | Common:14; Rare:93 | ||||
| chr11:71928930-71929079 | Common:1; Rare:49 | ||||
| chr11:72039769-72039848 | Rare:8 | ||||
| chr11:72040686-72040753 | Rare:14 | ||||
| chr11:72041056-72041209 | Common:1; Rare:25 | ||||
| chr11:72080238-72080341 | Common:6; Rare:15 |