| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:777465-777582 | Common:1; Rare:50 | ||||
| chr11:809825-810034 | Common:2; Rare:97 | ||||
| chr11:842497-842974 | Common:8; Rare:194 | ||||
| chr11:1309611-1309745 | Common:1; Rare:64 | ||||
| chr11:2992247-2992516 | Common:2; Rare:104 | ||||
| chr11:3797482-3797716 | Rare:91 | ||||
| chr11:3855555-3855687 | Common:2; Rare:28 | ||||
| chr11:4608166-4608405 | Common:1; Rare:67 | ||||
| chr11:5624951-5625005 | Rare:7 | ||||
| chr11:6234625-6234794 | Common:2; Rare:51 | ||||
| chr11:6319770-6319969 | Rare:49 | ||||
| chr11:6320481-6320638 | Common:2; Rare:53 | ||||
| chr11:6390241-6390502 | Common:2; Rare:74 | ||||
| chr11:6481292-6481539 | Common:4; Rare:106 | ||||
| chr11:6603548-6603835 | Common:4; Rare:85; Clinvar (benign):3 |