| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34438784-34439009 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr11:34916318-34916676 | Common:10; Rare:145; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138949-35139366 | Common:1; Rare:116 | ||||
| chr11:35525590-35525820 | Rare:54 | ||||
| chr11:35943969-35944111 | Common:2; Rare:46 | ||||
| chr11:36510236-36510382 | Rare:44 | ||||
| chr11:43358858-43358988 | Rare:62 | ||||
| chr11:45804965-45805170 | Common:2; Rare:48; Clinvar:4 | ||||
| chr11:45917851-45918158 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:46277903-46278089 | Rare:50 | ||||
| chr11:46617183-46617585 | Common:5; Rare:113 | ||||
| chr11:46700555-46700831 | Common:1; Rare:70 | ||||
| chr11:46700920-46701077 | Common:3; Rare:42 | ||||
| chr11:46846211-46846416 | Common:1; Rare:58 | ||||
| chr11:47214843-47215123 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):1 |