| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95186397-95186404 | Rare:1 | ||||
| chr11:95202730-95202899 | Rare:28 | ||||
| chr11:96166252-96166550 | Common:2; Rare:54 | ||||
| chr11:96224912-96225058 | Common:1; Rare:23 | ||||
| chr11:96243269-96243416 | Common:2; Rare:37 | ||||
| chr11:96307238-96307261 | Rare:4 | ||||
| chr11:96331889-96331954 | Rare:17 | ||||
| chr11:96341634-96341908 | Common:1; Rare:88 | ||||
| chr11:96341921-96342033 | Rare:16 | ||||
| chr11:101128259-101128357 | Rare:39 | ||||
| chr11:102401558-102401901 | Common:2; Rare:100 | ||||
| chr11:102448825-102448942 | Rare:34 | ||||
| chr11:105035960-105036101 | Common:1; Rare:16 | ||||
| chr11:106079767-106079967 | Common:2; Rare:33 | ||||
| chr11:108319709-108320004 | Rare:58; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 |