| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46380781-46381095 | Common:1; Rare:69 | ||||
| chr11:46617171-46617618 | Common:5; Rare:129 | ||||
| chr11:46700549-46700818 | Common:1; Rare:70 | ||||
| chr11:46846229-46846412 | Common:1; Rare:49 | ||||
| chr11:47186408-47186651 | Rare:54 | ||||
| chr11:47214816-47215094 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:47257362-47257633 | Common:3; Rare:50 | ||||
| chr11:47269994-47270198 | Common:1; Rare:73 | ||||
| chr11:47408354-47408646 | Common:1; Rare:92; Clinvar (benign):2 | ||||
| chr11:47565499-47565643 | Common:3; Rare:27 | ||||
| chr11:47578966-47579085 | Rare:61; Clinvar:2 | ||||
| chr11:47767270-47767657 | Common:1; Rare:127 | ||||
| chr11:47848322-47848406 | Rare:42 | ||||
| chr11:57324878-57325183 | Common:1; Rare:100 | ||||
| chr11:57530673-57530953 | Common:1; Rare:71 |