| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61816445-61816522 | Rare:25 | ||||
| chr11:61816784-61817187 | Common:1; Rare:92 | ||||
| chr11:61817348-61817395 | Rare:7 | ||||
| chr11:61827298-61827534 | Common:2; Rare:43 | ||||
| chr11:61827580-61827729 | Rare:28 | ||||
| chr11:61827852-61828131 | Common:1; Rare:41 | ||||
| chr11:61828185-61828424 | Rare:74 | ||||
| chr11:61828831-61829053 | Common:1; Rare:43 | ||||
| chr11:61891149-61891285 | Common:1; Rare:36 | ||||
| chr11:61891507-61891608 | Rare:37 | ||||
| chr11:61891776-61891827 | Common:1; Rare:16 | ||||
| chr11:61899125-61899378 | Common:1; Rare:66 | ||||
| chr11:61917553-61917664 | Common:1; Rare:36 | ||||
| chr11:61949284-61949478 | Rare:37 | ||||
| chr11:61949603-61950102 | Common:5; Rare:81; Clinvar (benign):3 |