| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74465329-74465459 | Common:1; Rare:34; Clinvar:1 | ||||
| chr2:74482904-74483120 | Common:1; Rare:78 | ||||
| chr2:74507263-74507518 | Rare:66 | ||||
| chr2:74507629-74507775 | Rare:37 | ||||
| chr2:74529654-74530009 | Rare:109; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74958876-74958944 | Rare:36 | ||||
| chr2:75561295-75561404 | Common:1; Rare:15 | ||||
| chr2:84459219-84459572 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905506-84905890 | Common:1; Rare:117 | ||||
| chr2:85327936-85328080 | Common:2; Rare:67 | ||||
| chr2:85354501-85354786 | Common:1; Rare:95 | ||||
| chr2:85538908-85539171 | Common:1; Rare:92 | ||||
| chr2:85561431-85561584 | Rare:57; Clinvar:4 | ||||
| chr2:85584369-85584467 | Common:1; Rare:36 | ||||
| chr2:85595555-85595802 | Common:2; Rare:88 |