| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67428163-67428537 | Rare:113 | ||||
| chr11:67440192-67440338 | Rare:50 | ||||
| chr11:67443458-67443733 | Common:2; Rare:91 | ||||
| chr11:67469212-67469417 | Common:1; Rare:65 | ||||
| chr11:67482901-67483154 | Rare:57; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67508100-67508211 | Common:1; Rare:39 | ||||
| chr11:67583655-67583844 | Common:1; Rare:63 | ||||
| chr11:67650209-67650351 | Common:2; Rare:33 | ||||
| chr11:68030380-68030733 | Common:3; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038919-68039090 | Rare:50; Clinvar:1 | ||||
| chr11:68271910-68272276 | Common:2; Rare:150 | ||||
| chr11:68460560-68460767 | Common:3; Rare:76 | ||||
| chr11:68839335-68839516 | Common:1; Rare:44 | ||||
| chr11:68903806-68903946 | Common:4; Rare:61; Clinvar (benign):6 | ||||
| chr11:69048646-69048944 | Common:5; Rare:92 |