| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:809799-810038 | Common:2; Rare:110 | ||||
| chr11:811877-811903 | Rare:3 | ||||
| chr11:818701-818994 | Common:1; Rare:63; Clinvar:1 | ||||
| chr11:819359-819961 | Common:4; Rare:202; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:820665-820730 | Rare:11 | ||||
| chr11:821223-821551 | Rare:64 | ||||
| chr11:822143-822567 | Common:1; Rare:124; Clinvar:6; Clinvar (pathogenic):2 | ||||
| chr11:832770-833022 | Common:7; Rare:83 | ||||
| chr11:842413-842984 | Common:8; Rare:231 | ||||
| chr11:843930-844442 | Common:4; Rare:145 | ||||
| chr11:846926-847245 | Rare:64 | ||||
| chr11:1036718-1036744 | Rare:5 | ||||
| chr11:1309566-1309851 | Common:2; Rare:119 | ||||
| chr11:1559215-1559436 | Common:2; Rare:56 | ||||
| chr11:1839973-1840259 | Common:1; Rare:63; Clinvar:1 |