| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46121113-46121317 | Common:2; Rare:36 | ||||
| chr11:46277444-46277665 | Rare:40 | ||||
| chr11:46380724-46381160 | Common:1; Rare:117 | ||||
| chr11:46617210-46617599 | Common:5; Rare:107 | ||||
| chr11:46700559-46700853 | Common:1; Rare:78 | ||||
| chr11:46846218-46846414 | Common:1; Rare:54 | ||||
| chr11:47176853-47177075 | Rare:91 | ||||
| chr11:47186368-47186536 | Rare:50 | ||||
| chr11:47214840-47215110 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248794-47248938 | Rare:56 | ||||
| chr11:47269550-47269684 | Common:1; Rare:46 | ||||
| chr11:47269981-47270172 | Common:1; Rare:65 | ||||
| chr11:47565478-47565643 | Common:3; Rare:32 | ||||
| chr11:47578952-47579087 | Rare:70; Clinvar:2 | ||||
| chr11:47848311-47848406 | Rare:51 |