| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69640651-69641328 | Common:2; Rare:249 | ||||
| chr11:69675278-69675534 | Common:1; Rare:134 | ||||
| chr11:70203092-70203395 | Common:7; Rare:206 | ||||
| chr11:70270424-70270775 | Common:4; Rare:260 | ||||
| chr11:70398174-70398640 | Common:7; Rare:234 | ||||
| chr11:71240880-71241230 | Rare:116 | ||||
| chr11:71241370-71241740 | Common:1; Rare:77 | ||||
| chr11:71448295-71448699 | Common:8; Rare:217; Clinvar:6; Clinvar (benign):2 | ||||
| chr11:71452981-71453318 | Common:6; Rare:194 | ||||
| chr11:71787280-71787551 | Common:32; Rare:204 | ||||
| chr11:71928386-71929072 | Common:2; Rare:345 | ||||
| chr11:72070054-72070191 | Rare:16 | ||||
| chr11:72080110-72080360 | Common:12; Rare:77 | ||||
| chr11:72080368-72080899 | Common:4; Rare:250; Clinvar:21 | ||||
| chr11:72103192-72103531 | Rare:190 |