| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:72080374-72080986 | Common:7; Rare:421; Clinvar:32 | ||||
| chr11:72103103-72103683 | Rare:343 | ||||
| chr11:72112050-72112559 | Common:1; Rare:304 | ||||
| chr11:72112648-72113082 | Common:11; Rare:349 | ||||
| chr11:72191851-72192224 | Rare:121; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:72223054-72223507 | Common:6; Rare:348 | ||||
| chr11:72223738-72224263 | Common:3; Rare:248 | ||||
| chr11:72224754-72224924 | Common:1; Rare:46 | ||||
| chr11:72224939-72225410 | Common:9; Rare:194; Clinvar (pathogenic):2 | ||||
| chr11:72434416-72434894 | Common:12; Rare:279; Clinvar (benign):3 | ||||
| chr11:72642250-72642690 | Common:4; Rare:95 | ||||
| chr11:72722234-72722652 | Rare:92 | ||||
| chr11:72752210-72752950 | Common:11; Rare:352 | ||||
| chr11:72755064-72756745 | Common:19; Rare:470 | ||||
| chr11:72781151-72781440 | Rare:205 |