| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3879909-3880355 | Common:2; Rare:138 | ||||
| chr11:3894171-3894700 | Common:1; Rare:177 | ||||
| chr11:3904659-3904987 | Common:4; Rare:75 | ||||
| chr11:3966982-3967728 | Common:2; Rare:183; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr11:4091267-4092698 | Common:10; Rare:435; Clinvar:18; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:5691994-5692444 | Common:7; Rare:136 | ||||
| chr11:5700362-5700762 | Common:12; Rare:84 | ||||
| chr11:5808658-5809058 | Common:10; Rare:151 | ||||
| chr11:5818555-5818955 | Common:13; Rare:157 | ||||
| chr11:5923199-5923360 | Rare:26 | ||||
| chr11:6201630-6201840 | Common:1; Rare:33 | ||||
| chr11:6203390-6203780 | Common:3; Rare:66 | ||||
| chr11:6378141-6378541 | Rare:83 | ||||
| chr11:6435742-6436142 | Common:3; Rare:94 | ||||
| chr11:6469130-6469422 | Rare:86 |