| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65570397-65570510 | Rare:52 | ||||
| chr11:65614216-65614445 | Rare:43 | ||||
| chr11:65615701-65615830 | Common:1; Rare:45 | ||||
| chr11:65662828-65663031 | Common:1; Rare:53 | ||||
| chr11:65663309-65663477 | Common:2; Rare:37 | ||||
| chr11:65712200-65712288 | Rare:28 | ||||
| chr11:65712401-65712633 | Common:2; Rare:76 | ||||
| chr11:65872682-65872998 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:65888368-65888676 | Common:1; Rare:104 | ||||
| chr11:65900322-65900540 | Common:3; Rare:42 | ||||
| chr11:65900546-65900549 | Rare:1 | ||||
| chr11:65961467-65961768 | Common:1; Rare:101 | ||||
| chr11:66002087-66002392 | Common:3; Rare:93; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:66002423-66002819 | Common:1; Rare:110; Clinvar:1 | ||||
| chr11:66257602-66257819 | Rare:60 |