| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74958776-74958910 | Rare:65 | ||||
| chr2:74958915-74959079 | Rare:43 | ||||
| chr2:75710864-75710944 | Common:1; Rare:29 | ||||
| chr2:84459181-84459583 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905494-84905927 | Common:2; Rare:132 | ||||
| chr2:85327931-85328291 | Common:7; Rare:124 | ||||
| chr2:85354558-85354790 | Common:1; Rare:68 | ||||
| chr2:85413979-85414098 | Common:1; Rare:26 | ||||
| chr2:85539028-85539197 | Common:2; Rare:76 | ||||
| chr2:85561424-85561575 | Rare:55; Clinvar:4 | ||||
| chr2:85595552-85595764 | Common:2; Rare:66 | ||||
| chr2:85602662-85602874 | Rare:52 | ||||
| chr2:85612038-85612103 | Rare:15 | ||||
| chr2:85888988-85889313 | Common:4; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:86105837-86105922 | Rare:30 |