| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:120128841-120129045 | Rare:43 | ||||
| chr11:120138144-120138451 | Common:3; Rare:73 | ||||
| chr11:120336201-120336480 | Rare:117 | ||||
| chr11:121292563-121292928 | Rare:111; Clinvar:3 | ||||
| chr11:123062066-123062295 | Common:5; Rare:96 | ||||
| chr11:123062402-123062663 | Common:4; Rare:120 | ||||
| chr11:123741634-123741769 | Rare:33 | ||||
| chr11:124622742-124622946 | Common:5; Rare:73 | ||||
| chr11:124673715-124673934 | Common:4; Rare:65 | ||||
| chr11:124953842-124954213 | Common:5; Rare:98 | ||||
| chr11:125164516-125164759 | Rare:45 | ||||
| chr11:125592451-125592917 | Common:6; Rare:158 | ||||
| chr11:125625653-125625806 | Rare:42 | ||||
| chr11:126211641-126211807 | Rare:76 | ||||
| chr11:126268769-126269207 | Common:2; Rare:169; Clinvar:2; Clinvar (benign):4 |