| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66907872-66908074 | Common:2; Rare:28 | ||||
| chr11:67303385-67303575 | Rare:48 | ||||
| chr11:67353269-67353386 | Rare:40 | ||||
| chr11:67353412-67353721 | Common:1; Rare:75 | ||||
| chr11:67428341-67428539 | Rare:69 | ||||
| chr11:67443438-67443598 | Common:1; Rare:58 | ||||
| chr11:67508038-67508225 | Common:1; Rare:58 | ||||
| chr11:67508621-67508766 | Common:3; Rare:51 | ||||
| chr11:68030381-68030785 | Common:3; Rare:111; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038919-68039060 | Rare:42; Clinvar:1 | ||||
| chr11:68271871-68272102 | Common:2; Rare:97 | ||||
| chr11:68460223-68460309 | Common:2; Rare:46 | ||||
| chr11:68903778-68903943 | Common:4; Rare:79; Clinvar (benign):6 | ||||
| chr11:69675300-69675448 | Rare:44 | ||||
| chr11:70398462-70398607 | Common:1; Rare:49 |