| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64354940-64355710 | Common:3; Rare:512 | ||||
| chr11:64358924-64359324 | Common:4; Rare:314 | ||||
| chr11:64555580-64556010 | Common:2; Rare:233 | ||||
| chr11:64712729-64712979 | Common:3; Rare:70 | ||||
| chr11:64742801-64743519 | Common:3; Rare:528; Clinvar:1 | ||||
| chr11:64743520-64743990 | Common:4; Rare:195 | ||||
| chr11:64744003-64744403 | Rare:114 | ||||
| chr11:64744482-64745379 | Common:2; Rare:892 | ||||
| chr11:64745335-64745562 | Rare:39 | ||||
| chr11:64745900-64746360 | Common:2; Rare:208 | ||||
| chr11:64754285-64754750 | Common:4; Rare:350; Clinvar:5; Clinvar (benign):12 | ||||
| chr11:64777500-64778154 | Common:4; Rare:576 | ||||
| chr11:64778438-64779346 | Common:44; Rare:1480 | ||||
| chr11:64802940-64803490 | Common:1; Rare:615 | ||||
| chr11:64803543-64803943 | Rare:121; Clinvar:2; Clinvar (pathogenic):2 |