| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:69675300-69675521 | Rare:61 | ||||
| chr11:70398333-70398614 | Common:2; Rare:98 | ||||
| chr11:71448288-71448794 | Common:5; Rare:129; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:71928907-71929058 | Common:1; Rare:50 | ||||
| chr11:72080453-72080634 | Common:1; Rare:37; Clinvar:3 | ||||
| chr11:72103199-72103498 | Rare:84 | ||||
| chr11:72112264-72112452 | Rare:45 | ||||
| chr11:72112641-72112958 | Common:4; Rare:134 | ||||
| chr11:72752345-72752519 | Common:2; Rare:55 | ||||
| chr11:72814070-72814432 | Common:1; Rare:105 | ||||
| chr11:72822147-72822431 | Common:1; Rare:112 | ||||
| chr11:73598049-73598281 | Common:3; Rare:60 | ||||
| chr11:73787781-73787946 | Common:1; Rare:38 | ||||
| chr11:73876767-73877036 | Common:5; Rare:76 | ||||
| chr11:74170845-74171418 | Common:3; Rare:183 |