| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64318066-64318228 | Rare:66 | ||||
| chr11:64778479-64778767 | Common:1; Rare:119 | ||||
| chr11:64917207-64917393 | Rare:48 | ||||
| chr11:65014028-65014258 | Rare:56 | ||||
| chr11:65084028-65084272 | Common:1; Rare:72 | ||||
| chr11:65134503-65134560 | Common:1; Rare:11 | ||||
| chr11:65261759-65261989 | Common:3; Rare:66 | ||||
| chr11:65333617-65333881 | Common:1; Rare:113 | ||||
| chr11:65570350-65570483 | Rare:54 | ||||
| chr11:65662902-65663095 | Common:1; Rare:48 | ||||
| chr11:65712156-65712270 | Rare:44 | ||||
| chr11:65720482-65720578 | Common:1; Rare:54 | ||||
| chr11:65888419-65888686 | Common:1; Rare:93 | ||||
| chr11:66002134-66002561 | Common:3; Rare:117; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:66049120-66049327 | Common:2; Rare:37 |