| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67469229-67469384 | Common:1; Rare:45 | ||||
| chr11:67482941-67483171 | Rare:51; Clinvar:1; Clinvar (benign):3 | ||||
| chr11:67508071-67508441 | Common:1; Rare:79 | ||||
| chr11:67583662-67583864 | Common:1; Rare:72 | ||||
| chr11:68010143-68010354 | Common:1; Rare:54 | ||||
| chr11:68030384-68030751 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038915-68039064 | Rare:44; Clinvar:1 | ||||
| chr11:68213921-68213977 | Rare:32 | ||||
| chr11:68271895-68272123 | Common:2; Rare:95 | ||||
| chr11:68460222-68460423 | Common:3; Rare:69 | ||||
| chr11:68903778-68903943 | Common:4; Rare:79; Clinvar (benign):6 | ||||
| chr11:69013166-69013433 | Common:4; Rare:80 | ||||
| chr11:69048601-69048960 | Common:5; Rare:107 | ||||
| chr11:69675309-69675486 | Rare:49 | ||||
| chr11:70078406-70078597 | Rare:49 |