| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69675300-69675519 | Rare:60 | ||||
| chr11:70398364-70398607 | Common:2; Rare:87 | ||||
| chr11:71448300-71448702 | Common:4; Rare:110; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71787350-71787548 | Common:12; Rare:84 | ||||
| chr11:72041056-72041331 | Common:1; Rare:50 | ||||
| chr11:72041496-72041595 | Rare:13 | ||||
| chr11:72080449-72080867 | Common:2; Rare:93; Clinvar:8 | ||||
| chr11:72103199-72103518 | Rare:93 | ||||
| chr11:72112223-72112508 | Rare:73 | ||||
| chr11:72112656-72112871 | Common:3; Rare:93 | ||||
| chr11:72814064-72814432 | Common:2; Rare:106 | ||||
| chr11:73598049-73598287 | Common:3; Rare:62 | ||||
| chr11:73760158-73760318 | Rare:30 | ||||
| chr11:73760577-73760762 | Common:2; Rare:45 | ||||
| chr11:73787782-73787974 | Common:1; Rare:50 |