| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61392335-61392686 | Common:2; Rare:86; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:61392765-61392864 | Rare:22 | ||||
| chr11:61429341-61429583 | Common:2; Rare:74 | ||||
| chr11:61429842-61430279 | Common:2; Rare:174; Clinvar:3; Clinvar (benign):9 | ||||
| chr11:61508496-61508811 | Common:1; Rare:84 | ||||
| chr11:61509178-61509570 | Common:1; Rare:89 | ||||
| chr11:61581041-61581117 | Common:1; Rare:12 | ||||
| chr11:61680240-61680481 | Common:1; Rare:76 | ||||
| chr11:61752460-61752673 | Common:2; Rare:56 | ||||
| chr11:61792044-61792364 | Rare:62 | ||||
| chr11:61792453-61792734 | Common:5; Rare:121 | ||||
| chr11:61792824-61793044 | Rare:47 | ||||
| chr11:61814568-61814845 | Common:1; Rare:57 | ||||
| chr11:61815053-61815722 | Common:6; Rare:139 | ||||
| chr11:61816111-61816396 | Rare:79 |