| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73787752-73787950 | Common:2; Rare:82 | ||||
| chr11:73788000-73788400 | Common:11; Rare:126 | ||||
| chr11:73876493-73877049 | Common:10; Rare:240 | ||||
| chr11:73982759-73982965 | Common:7; Rare:75 | ||||
| chr11:73983160-73983590 | Common:7; Rare:164 | ||||
| chr11:74170830-74171522 | Common:7; Rare:410 | ||||
| chr11:74269080-74269600 | Common:4; Rare:86 | ||||
| chr11:74398380-74398573 | Common:6; Rare:82 | ||||
| chr11:74493050-74493409 | Common:2; Rare:227; Clinvar (pathogenic):2 | ||||
| chr11:74493660-74493845 | Common:2; Rare:142 | ||||
| chr11:74592486-74592692 | Common:2; Rare:126 | ||||
| chr11:74697470-74697760 | Common:6; Rare:94 | ||||
| chr11:74697710-74698120 | Common:6; Rare:81 | ||||
| chr11:74748654-74748889 | Common:6; Rare:107 | ||||
| chr11:74748900-74749810 | Common:12; Rare:348 |