| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75710669-75710778 | Common:2; Rare:42 | ||||
| chr2:75710872-75711113 | Common:1; Rare:73 | ||||
| chr2:84459226-84459572 | Common:3; Rare:89; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905506-84905954 | Common:1; Rare:135 | ||||
| chr2:85327636-85327847 | Common:4; Rare:62 | ||||
| chr2:85327915-85328080 | Common:2; Rare:74 | ||||
| chr2:85354491-85354792 | Common:1; Rare:100 | ||||
| chr2:85539024-85539207 | Common:3; Rare:86 | ||||
| chr2:85561425-85561581 | Rare:58; Clinvar:4 | ||||
| chr2:85584317-85584466 | Common:1; Rare:44 | ||||
| chr2:85595558-85595809 | Common:1; Rare:89 | ||||
| chr2:85602629-85602904 | Rare:72 | ||||
| chr2:85611960-85612104 | Rare:60 | ||||
| chr2:85753435-85753738 | Common:2; Rare:71 | ||||
| chr2:85888872-85889151 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):2 |