| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85612030-85612086 | Rare:17 | ||||
| chr2:85616130-85616186 | Rare:25 | ||||
| chr2:86105828-86106186 | Common:2; Rare:93 | ||||
| chr2:86195393-86195674 | Common:6; Rare:91 | ||||
| chr2:86199403-86199512 | Common:1; Rare:47 | ||||
| chr2:88055726-88055888 | Rare:59 | ||||
| chr2:95165651-95165828 | Rare:54 | ||||
| chr2:96265972-96266306 | Common:2; Rare:96; Clinvar:1 | ||||
| chr2:96305475-96305625 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:96335723-96335813 | Common:1; Rare:30 | ||||
| chr2:97094848-97094973 | Common:1; Rare:24 | ||||
| chr2:97645829-97646089 | Common:2; Rare:79 | ||||
| chr2:98608447-98608636 | Common:1; Rare:82 | ||||
| chr2:99141554-99141592 | Common:1; Rare:19 | ||||
| chr2:99154888-99155040 | Common:1; Rare:63; Clinvar (benign):2 |