| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:70398455-70398614 | Common:1; Rare:56 | ||||
| chr11:71448338-71448690 | Common:4; Rare:94; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928862-71929073 | Common:1; Rare:70 | ||||
| chr11:72041850-72041893 | Rare:8 | ||||
| chr11:72080471-72080648 | Rare:35; Clinvar:2 | ||||
| chr11:72080691-72080958 | Rare:69; Clinvar:4 | ||||
| chr11:72112256-72112550 | Rare:72 | ||||
| chr11:72752396-72752620 | Common:2; Rare:63 | ||||
| chr11:72814248-72814446 | Common:2; Rare:65 | ||||
| chr11:73760567-73761130 | Common:5; Rare:152 | ||||
| chr11:73876767-73877036 | Common:5; Rare:76 | ||||
| chr11:74170842-74171367 | Common:2; Rare:165 | ||||
| chr11:74398378-74398558 | Common:3; Rare:40 | ||||
| chr11:74949055-74949328 | Common:6; Rare:83 | ||||
| chr11:75562159-75562313 | Common:1; Rare:43; Clinvar:3; Clinvar (benign):1 |