| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66593042-66593236 | Common:1; Rare:70 | ||||
| chr11:66616422-66616646 | Common:1; Rare:59 | ||||
| chr11:66638417-66638735 | Common:4; Rare:136 | ||||
| chr11:66677765-66678065 | Common:1; Rare:111 | ||||
| chr11:66744650-66744887 | Common:3; Rare:97 | ||||
| chr11:66907857-66908065 | Common:2; Rare:29 | ||||
| chr11:67240143-67240309 | Rare:32 | ||||
| chr11:67303343-67303582 | Rare:61 | ||||
| chr11:67353485-67353721 | Common:1; Rare:62 | ||||
| chr11:67399125-67399445 | Common:2; Rare:74 | ||||
| chr11:67401735-67402101 | Common:3; Rare:134 | ||||
| chr11:67428317-67428537 | Rare:74 | ||||
| chr11:67443458-67443710 | Common:2; Rare:87 | ||||
| chr11:67482936-67483171 | Rare:53; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67583566-67583862 | Common:2; Rare:87 |