| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:28820356-28820572 | Rare:46 | ||||
| chr11:28833220-28833382 | Common:4; Rare:24 | ||||
| chr11:28833629-28834136 | Common:7; Rare:88 | ||||
| chr11:28834895-28835142 | Common:4; Rare:48 | ||||
| chr11:28836282-28836709 | Common:3; Rare:73 | ||||
| chr11:28836774-28836964 | Common:5; Rare:40 | ||||
| chr11:28838794-28838902 | Common:1; Rare:19 | ||||
| chr11:28839238-28839373 | Common:1; Rare:22 | ||||
| chr11:28861043-28861128 | Rare:16 | ||||
| chr11:29160145-29160173 | Rare:6 | ||||
| chr11:34654014-34654245 | Rare:40 | ||||
| chr11:35663315-35663339 | Rare:11 | ||||
| chr11:36372461-36372604 | Rare:23 | ||||
| chr11:36374390-36374513 | Rare:12 | ||||
| chr11:45914183-45914373 | Rare:69; Clinvar:5; Clinvar (pathogenic):1 |