| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67469098-67469433 | Common:3; Rare:113 | ||||
| chr11:67482907-67483164 | Rare:57; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67498520-67498681 | Common:1; Rare:59 | ||||
| chr11:67498809-67498962 | Rare:45 | ||||
| chr11:67508044-67508417 | Common:1; Rare:87 | ||||
| chr11:67508654-67508751 | Common:1; Rare:34 | ||||
| chr11:68010174-68010359 | Common:1; Rare:47 | ||||
| chr11:68030370-68030519 | Rare:47 | ||||
| chr11:68030594-68030964 | Common:7; Rare:108; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68032048-68032235 | Common:1; Rare:54; Clinvar:1 | ||||
| chr11:68038926-68039110 | Rare:55; Clinvar:1 | ||||
| chr11:68043618-68043858 | Common:1; Rare:84; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:68049209-68049391 | Rare:65; Clinvar:1 | ||||
| chr11:68121373-68121590 | Common:1; Rare:60 | ||||
| chr11:68213145-68213447 | Common:2; Rare:126 |