| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65961523-65962012 | Common:1; Rare:151 | ||||
| chr11:66002097-66002287 | Common:1; Rare:59; Clinvar:5; Clinvar (benign):1 | ||||
| chr11:66002345-66002826 | Common:1; Rare:127; Clinvar:1 | ||||
| chr11:66011913-66012032 | Rare:30 | ||||
| chr11:66026472-66026560 | Rare:11 | ||||
| chr11:66052204-66052606 | Common:4; Rare:133 | ||||
| chr11:66058054-66058402 | Rare:88 | ||||
| chr11:66257577-66257875 | Common:1; Rare:84 | ||||
| chr11:66268404-66268679 | Common:3; Rare:80 | ||||
| chr11:66268809-66268858 | Common:2; Rare:17 | ||||
| chr11:66288992-66289310 | Common:1; Rare:81 | ||||
| chr11:66344829-66345248 | Common:2; Rare:96 | ||||
| chr11:66347605-66347890 | Common:5; Rare:68 | ||||
| chr11:66420830-66421039 | Common:1; Rare:58 | ||||
| chr11:66438753-66439081 | Common:2; Rare:84 |