| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74529668-74530050 | Rare:112; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74553899-74554165 | Rare:54 | ||||
| chr2:74833823-74834147 | Common:1; Rare:96 | ||||
| chr2:75561282-75561608 | Common:2; Rare:44 | ||||
| chr2:84459180-84459583 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905560-84905834 | Common:1; Rare:86 | ||||
| chr2:85327919-85328055 | Common:1; Rare:63 | ||||
| chr2:85354501-85354807 | Common:1; Rare:105 | ||||
| chr2:85539019-85539369 | Common:3; Rare:169; Clinvar (benign):7 | ||||
| chr2:85561403-85561543 | Rare:54; Clinvar:5 | ||||
| chr2:85595577-85595773 | Common:1; Rare:69 | ||||
| chr2:85602662-85602915 | Rare:60 | ||||
| chr2:85612024-85612103 | Rare:23 | ||||
| chr2:85888956-85889262 | Common:4; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:86105777-86106332 | Common:4; Rare:193 |