| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:832858-833022 | Common:7; Rare:60 | ||||
| chr11:837057-837615 | Common:6; Rare:199 | ||||
| chr11:837737-838025 | Common:1; Rare:90 | ||||
| chr11:842446-842978 | Common:8; Rare:220 | ||||
| chr11:843937-844442 | Common:4; Rare:142 | ||||
| chr11:1222960-1223180 | Common:2; Rare:66 | ||||
| chr11:1309528-1309851 | Common:3; Rare:135 | ||||
| chr11:1759334-1759665 | Common:3; Rare:92; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr11:1834248-1834492 | Rare:55 | ||||
| chr11:2301867-2302131 | Common:2; Rare:69 | ||||
| chr11:2902065-2902359 | Common:1; Rare:68 | ||||
| chr11:3057368-3057545 | Rare:62 | ||||
| chr11:3165247-3165397 | Common:1; Rare:45 | ||||
| chr11:3379096-3379199 | Common:2; Rare:31 | ||||
| chr11:3641984-3642189 | Common:7; Rare:73 |