| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67611919-67612145 | Common:2; Rare:82; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr11:68010130-68010371 | Common:1; Rare:62 | ||||
| chr11:68030412-68030795 | Common:3; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038915-68039101 | Rare:54; Clinvar:1 | ||||
| chr11:68043623-68043818 | Common:1; Rare:63; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr11:68271881-68272148 | Common:2; Rare:112 | ||||
| chr11:68460223-68460516 | Common:3; Rare:95 | ||||
| chr11:68903774-68903943 | Common:4; Rare:80; Clinvar (benign):6 | ||||
| chr11:69013191-69013466 | Common:2; Rare:79 | ||||
| chr11:69048703-69048975 | Common:5; Rare:94 | ||||
| chr11:69640983-69641259 | Common:1; Rare:58 | ||||
| chr11:69675300-69675488 | Rare:54 | ||||
| chr11:70203163-70203343 | Common:2; Rare:69 | ||||
| chr11:70398342-70398611 | Common:2; Rare:96 | ||||
| chr11:70826510-70826578 | Rare:20 |