| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61977418-61977538 | Rare:20 | ||||
| chr11:62801163-62801249 | Rare:31 | ||||
| chr11:63996745-63997149 | Common:4; Rare:114 | ||||
| chr11:64036437-64036582 | Rare:25 | ||||
| chr11:64236164-64236327 | Common:1; Rare:68 | ||||
| chr11:64758255-64758504 | Common:1; Rare:73; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr11:65416495-65416644 | Common:1; Rare:43 | ||||
| chr11:65418705-65418955 | Common:2; Rare:48 | ||||
| chr11:65420014-65420187 | Rare:41 | ||||
| chr11:65421096-65421508 | Rare:86 | ||||
| chr11:65422175-65422473 | Common:1; Rare:111 | ||||
| chr11:65422647-65423082 | Common:3; Rare:121 | ||||
| chr11:65423089-65423687 | Common:3; Rare:148 | ||||
| chr11:65423754-65424742 | Common:3; Rare:202 | ||||
| chr11:65425182-65425693 | Rare:91 |