| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74482916-74483098 | Common:1; Rare:60 | ||||
| chr2:74483230-74483387 | Common:1; Rare:63 | ||||
| chr2:74507356-74507545 | Rare:56 | ||||
| chr2:74507669-74507879 | Common:1; Rare:58 | ||||
| chr2:74529668-74529938 | Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74958498-74958677 | Common:3; Rare:64 | ||||
| chr2:74958872-74959029 | Rare:60 | ||||
| chr2:75646571-75646853 | Common:1; Rare:84 | ||||
| chr2:75710625-75710761 | Common:1; Rare:56 | ||||
| chr2:75711194-75711204 | Rare:1 | ||||
| chr2:84459192-84459606 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:85327915-85328084 | Common:2; Rare:76 | ||||
| chr2:85354526-85354807 | Common:1; Rare:93 | ||||
| chr2:85413986-85414183 | Common:2; Rare:38 | ||||
| chr2:85539068-85539200 | Common:2; Rare:60 |