| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:9575486-9575635 | Common:1; Rare:25 | ||||
| chr11:9663883-9664217 | Common:4; Rare:107 | ||||
| chr11:10304908-10305088 | Common:1; Rare:39 | ||||
| chr11:10455137-10455432 | Common:5; Rare:55; Clinvar:2; Clinvar (benign):6 | ||||
| chr11:10456239-10456328 | Rare:19 | ||||
| chr11:10541134-10541331 | Rare:74 | ||||
| chr11:10693484-10693700 | Common:1; Rare:69 | ||||
| chr11:10693906-10694150 | Rare:33 | ||||
| chr11:10750697-10751019 | Common:4; Rare:85 | ||||
| chr11:10751115-10751345 | Rare:71 | ||||
| chr11:10798996-10799431 | Common:3; Rare:147 | ||||
| chr11:10804123-10804416 | Rare:71 | ||||
| chr11:10808704-10808787 | Rare:22 | ||||
| chr11:10808853-10809013 | Common:1; Rare:73 | ||||
| chr11:10858013-10858283 | Common:3; Rare:87 |