| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68460165-68460349 | Common:2; Rare:88 | ||||
| chr11:68460504-68460869 | Common:3; Rare:122 | ||||
| chr11:68460925-68460986 | Rare:29 | ||||
| chr11:68461002-68461078 | Rare:23 | ||||
| chr11:68461145-68461488 | Common:5; Rare:116 | ||||
| chr11:68684504-68684615 | Rare:36 | ||||
| chr11:68750978-68751138 | Common:2; Rare:13 | ||||
| chr11:68751295-68751728 | Common:1; Rare:91 | ||||
| chr11:68839057-68839191 | Rare:18 | ||||
| chr11:68839224-68839525 | Common:2; Rare:66 | ||||
| chr11:68841905-68842015 | Rare:28 | ||||
| chr11:68843877-68844168 | Common:1; Rare:54 | ||||
| chr11:68903713-68904041 | Common:6; Rare:132; Clinvar:6; Clinvar (benign):8 | ||||
| chr11:69048676-69049129 | Common:7; Rare:144 | ||||
| chr11:69049344-69049630 | Common:4; Rare:61 |