| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74147866-74148140 | Common:1; Rare:69; Clinvar:2 | ||||
| chr2:74178774-74179026 | Common:2; Rare:67 | ||||
| chr2:74440429-74440685 | Rare:69 | ||||
| chr2:74482902-74483113 | Common:1; Rare:73 | ||||
| chr2:74507669-74507789 | Rare:25 | ||||
| chr2:74529659-74530013 | Rare:106; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74554666-74554755 | Common:1; Rare:37 | ||||
| chr2:74958483-74958671 | Common:2; Rare:65 | ||||
| chr2:74958872-74959079 | Rare:73 | ||||
| chr2:84459226-84459581 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905517-84905718 | Common:1; Rare:64 | ||||
| chr2:85327916-85328094 | Common:3; Rare:80 | ||||
| chr2:85354517-85354799 | Common:1; Rare:93 | ||||
| chr2:85539057-85539168 | Common:1; Rare:43 | ||||
| chr2:85561447-85561581 | Rare:49; Clinvar:4 |