| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66561048-66561329 | Common:3; Rare:68 | ||||
| chr11:66790628-66790790 | Rare:21 | ||||
| chr11:66791842-66792168 | Common:1; Rare:55 | ||||
| chr11:67117717-67117790 | Common:1; Rare:16 | ||||
| chr11:67612256-67612450 | Common:2; Rare:67; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:67620177-67620242 | Common:2; Rare:24 | ||||
| chr11:67620853-67621004 | Rare:28 | ||||
| chr11:67625877-67626132 | Rare:43 | ||||
| chr11:67627297-67627326 | Rare:9 | ||||
| chr11:67629363-67629414 | Rare:13 | ||||
| chr11:67805342-67805579 | Common:3; Rare:87 | ||||
| chr11:67996799-67996989 | Rare:51 | ||||
| chr11:68682844-68683059 | Common:2; Rare:31 | ||||
| chr11:69965913-69966042 | Common:1; Rare:29 | ||||
| chr11:70219920-70220059 | Common:1; Rare:22 |