| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67460052-67460213 | Common:1; Rare:31; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:67460336-67460398 | Common:1; Rare:10; Clinvar (benign):1 | ||||
| chr11:67484454-67484553 | Rare:22 | ||||
| chr11:67484873-67484991 | Common:1; Rare:22 | ||||
| chr11:67485884-67486125 | Common:1; Rare:38 | ||||
| chr11:67486129-67486207 | Common:1; Rare:14 | ||||
| chr11:67558124-67558307 | Common:1; Rare:32 | ||||
| chr11:67562028-67562366 | Common:6; Rare:50 | ||||
| chr11:67582752-67582814 | Rare:12 | ||||
| chr11:67588000-67588118 | Rare:21 | ||||
| chr11:67600478-67600670 | Common:1; Rare:37 | ||||
| chr11:67614041-67614565 | Common:1; Rare:106 | ||||
| chr11:67648266-67648495 | Common:5; Rare:41 | ||||
| chr11:67648982-67649104 | Common:1; Rare:24 | ||||
| chr11:67805243-67805584 | Common:3; Rare:136 |