| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73331370-73331828 | Common:3; Rare:111 | ||||
| chr11:73779347-73779830 | Common:2; Rare:218 | ||||
| chr11:73784320-73784690 | Common:4; Rare:92 | ||||
| chr11:74138464-74138955 | Common:2; Rare:199; Clinvar:2 | ||||
| chr11:75155770-75156370 | Common:10; Rare:171 | ||||
| chr11:75168680-75169230 | Common:5; Rare:183 | ||||
| chr11:75352234-75352507 | Common:1; Rare:89 | ||||
| chr11:75404170-75404426 | Rare:62 | ||||
| chr11:75554454-75554886 | Common:8; Rare:173 | ||||
| chr11:75565363-75565960 | Common:10; Rare:145 | ||||
| chr11:75782549-75783319 | Common:7; Rare:241 | ||||
| chr11:75795701-75796148 | Common:2; Rare:208 | ||||
| chr11:76208899-76209076 | Common:2; Rare:72 | ||||
| chr11:76769747-76769924 | Rare:30 | ||||
| chr11:77172430-77172840 | Common:2; Rare:192; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):3 |