| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3855555-3855760 | Common:2; Rare:44 | ||||
| chr11:3856063-3856308 | Rare:77; Clinvar:1 | ||||
| chr11:4393654-4393801 | Rare:35 | ||||
| chr11:5624903-5625023 | Rare:15 | ||||
| chr11:6234623-6234878 | Common:2; Rare:77 | ||||
| chr11:6319753-6319788 | Rare:11 | ||||
| chr11:6320093-6320228 | Common:2; Rare:59 | ||||
| chr11:6320487-6320749 | Common:2; Rare:72 | ||||
| chr11:6390243-6390517 | Common:2; Rare:80 | ||||
| chr11:6473879-6474124 | Rare:74 | ||||
| chr11:6481292-6481530 | Common:4; Rare:99 | ||||
| chr11:6603462-6603899 | Common:4; Rare:135; Clinvar (benign):3 | ||||
| chr11:6619219-6619359 | Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:6619371-6619560 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:6683241-6683634 | Common:6; Rare:153 |