| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64317393-64317852 | Common:6; Rare:139 | ||||
| chr11:64317959-64318361 | Common:1; Rare:164 | ||||
| chr11:64318673-64318726 | Rare:7 | ||||
| chr11:64358946-64359264 | Common:1; Rare:83 | ||||
| chr11:64359488-64359551 | Rare:15 | ||||
| chr11:64555696-64555990 | Rare:77 | ||||
| chr11:64713464-64713527 | Rare:18; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:64742933-64743133 | Rare:67 | ||||
| chr11:64743675-64743851 | Common:1; Rare:41 | ||||
| chr11:64777676-64778046 | Common:1; Rare:160 | ||||
| chr11:64778389-64779210 | Common:7; Rare:302 | ||||
| chr11:64803147-64803441 | Rare:113 | ||||
| chr11:64803614-64803777 | Rare:48 | ||||
| chr11:64810505-64810876 | Common:4; Rare:89; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:64844595-64844924 | Common:4; Rare:93 |