| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46700564-46700812 | Common:1; Rare:63 | ||||
| chr11:46846258-46846314 | Rare:16 | ||||
| chr11:47214837-47215123 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248794-47248957 | Rare:66 | ||||
| chr11:47378326-47378634 | Rare:86 | ||||
| chr11:47565496-47565615 | Common:2; Rare:24 | ||||
| chr11:47578959-47579136 | Rare:94; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47594330-47594464 | Common:1; Rare:36 | ||||
| chr11:47642448-47642721 | Rare:109 | ||||
| chr11:47767293-47767649 | Common:1; Rare:114 | ||||
| chr11:47848305-47848406 | Rare:55 | ||||
| chr11:57427023-57427237 | Common:1; Rare:67 | ||||
| chr11:57514600-57514949 | Rare:64 | ||||
| chr11:57515214-57515245 | Rare:6 | ||||
| chr11:57530678-57530853 | Common:1; Rare:42 |