| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64359083-64359171 | Rare:20 | ||||
| chr11:64643545-64643808 | Common:2; Rare:59 | ||||
| chr11:64759905-64760079 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:64803145-64803339 | Rare:84 | ||||
| chr11:64810502-64810821 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:64917200-64917573 | Common:3; Rare:84 | ||||
| chr11:64990263-64990346 | Rare:10 | ||||
| chr11:65014001-65014237 | Rare:67 | ||||
| chr11:65027742-65027865 | Common:2; Rare:39 | ||||
| chr11:65040815-65040944 | Common:1; Rare:35 | ||||
| chr11:65083980-65084286 | Common:2; Rare:100 | ||||
| chr11:65096064-65096253 | Common:1; Rare:56 | ||||
| chr11:65134480-65134579 | Common:1; Rare:25 | ||||
| chr11:65134812-65134818 | Rare:2 | ||||
| chr11:65261739-65262002 | Common:4; Rare:80 |