| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75646694-75647142 | Common:3; Rare:134 | ||||
| chr2:75710872-75711061 | Common:1; Rare:62 | ||||
| chr2:77521681-77521942 | Common:1; Rare:52 | ||||
| chr2:84459194-84459604 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84516178-84516548 | Common:2; Rare:97 | ||||
| chr2:84904924-84905347 | Common:2; Rare:86 | ||||
| chr2:84905469-84905840 | Common:2; Rare:115 | ||||
| chr2:84906575-84906763 | Common:2; Rare:30 | ||||
| chr2:85327919-85328105 | Common:3; Rare:86 | ||||
| chr2:85354526-85354807 | Common:1; Rare:93 | ||||
| chr2:85430812-85431156 | Common:7; Rare:71 | ||||
| chr2:85538718-85539177 | Common:3; Rare:143 | ||||
| chr2:85561424-85561538 | Rare:44; Clinvar:4 | ||||
| chr2:85595552-85595838 | Common:2; Rare:98 | ||||
| chr2:85602663-85602951 | Rare:66 |