| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85616020-85616296 | Common:1; Rare:105 | ||||
| chr2:85888872-85889157 | Common:2; Rare:95; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:86105843-86106263 | Common:3; Rare:122 | ||||
| chr2:86195348-86195691 | Common:8; Rare:108 | ||||
| chr2:88055722-88056060 | Common:1; Rare:110 | ||||
| chr2:88691474-88691706 | Common:2; Rare:78 | ||||
| chr2:95165397-95165431 | Rare:3 | ||||
| chr2:95165645-95165822 | Rare:54 | ||||
| chr2:95402607-95402757 | Rare:50 | ||||
| chr2:96208252-96208467 | Rare:105 | ||||
| chr2:96208816-96208950 | Common:3; Rare:48 | ||||
| chr2:96265967-96266348 | Common:2; Rare:115; Clinvar:1 | ||||
| chr2:96305449-96305640 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96335706-96335813 | Common:1; Rare:35 | ||||
| chr2:96638292-96638445 | Common:1; Rare:39 |