| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61792564-61792947 | Common:5; Rare:105 | ||||
| chr11:61967311-61967783 | Common:3; Rare:178; Clinvar:4 | ||||
| chr11:62123795-62124073 | Common:6; Rare:70 | ||||
| chr11:62337323-62337526 | Common:4; Rare:65 | ||||
| chr11:62545583-62545987 | Common:1; Rare:94 | ||||
| chr11:62546673-62546917 | Common:1; Rare:78 | ||||
| chr11:62646563-62646778 | Common:1; Rare:88; Clinvar (pathogenic):1 | ||||
| chr11:62653262-62653447 | Common:1; Rare:62 | ||||
| chr11:62665139-62665434 | Common:6; Rare:142 | ||||
| chr11:62678883-62679225 | Rare:110 | ||||
| chr11:62706228-62706445 | Common:3; Rare:97; Clinvar (benign):5 | ||||
| chr11:62707341-62707649 | Common:3; Rare:69 | ||||
| chr11:62709517-62709659 | Rare:62 | ||||
| chr11:62727455-62727698 | Rare:92 | ||||
| chr11:62727913-62728138 | Common:5; Rare:44 |