| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1763794-1764019 | Rare:85; Clinvar:11; Clinvar (benign):8 | ||||
| chr11:1834227-1834599 | Common:1; Rare:89 | ||||
| chr11:2377384-2377615 | Common:3; Rare:71; Clinvar:1 | ||||
| chr11:2903483-2903505 | Common:1; Rare:7 | ||||
| chr11:3057344-3057540 | Rare:72 | ||||
| chr11:3797497-3797982 | Rare:178 | ||||
| chr11:3854356-3854662 | Rare:60 | ||||
| chr11:3855547-3855715 | Common:2; Rare:32 | ||||
| chr11:3856246-3856396 | Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:4094687-4094971 | Common:1; Rare:72 | ||||
| chr11:4393650-4393808 | Rare:40 | ||||
| chr11:5624894-5625052 | Rare:27 | ||||
| chr11:5690887-5691012 | Common:1; Rare:22 | ||||
| chr11:6319709-6319992 | Common:1; Rare:72 | ||||
| chr11:6320412-6320435 | Rare:9 |