| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68271947-68272260 | Common:2; Rare:134 | ||||
| chr11:68312285-68312685 | Common:2; Rare:258 | ||||
| chr11:68312596-68313384 | Common:8; Rare:286; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:68460530-68460808 | Common:3; Rare:99 | ||||
| chr11:68684448-68684548 | Common:1; Rare:25 | ||||
| chr11:68751415-68751705 | Common:1; Rare:59 | ||||
| chr11:68839329-68839488 | Common:1; Rare:39 | ||||
| chr11:68843939-68844157 | Common:1; Rare:40 | ||||
| chr11:68903776-68903986 | Common:5; Rare:97; Clinvar:4; Clinvar (benign):7 | ||||
| chr11:69048701-69049003 | Common:6; Rare:107 | ||||
| chr11:69293981-69294184 | Common:3; Rare:27 | ||||
| chr11:69640928-69641185 | Rare:54 | ||||
| chr11:69675151-69675624 | Common:3; Rare:139 | ||||
| chr11:69703991-69704244 | Rare:56 | ||||
| chr11:69704599-69704754 | Rare:41 |