| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17351875-17352039 | Common:2; Rare:38 | ||||
| chr11:17352234-17352314 | Common:1; Rare:13 | ||||
| chr11:17533830-17534073 | Common:2; Rare:41 | ||||
| chr11:17544347-17544512 | Common:3; Rare:40; Clinvar:2 | ||||
| chr11:18012910-18013234 | Common:6; Rare:108 | ||||
| chr11:18106003-18106309 | Common:3; Rare:104 | ||||
| chr11:18322058-18322306 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322447-18322661 | Common:2; Rare:79 | ||||
| chr11:18394393-18394641 | Common:1; Rare:97; Clinvar (benign):1 | ||||
| chr11:18412213-18412327 | Common:2; Rare:48 | ||||
| chr11:18526835-18527056 | Common:2; Rare:107 | ||||
| chr11:18588661-18588937 | Common:3; Rare:90 | ||||
| chr11:18634326-18634574 | Common:2; Rare:79 | ||||
| chr11:18634759-18634887 | Common:1; Rare:32 | ||||
| chr11:20022669-20023073 | Common:1; Rare:68 |