| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74482916-74483120 | Common:1; Rare:75 | ||||
| chr2:74507639-74507852 | Rare:51 | ||||
| chr2:74529668-74530009 | Rare:99; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74553947-74554086 | Rare:22 | ||||
| chr2:74554406-74554757 | Common:2; Rare:104 | ||||
| chr2:74555624-74555798 | Common:1; Rare:50 | ||||
| chr2:74958613-74958694 | Common:1; Rare:39 | ||||
| chr2:74958872-74959081 | Rare:74 | ||||
| chr2:75710669-75710778 | Common:2; Rare:42 | ||||
| chr2:84459226-84459581 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905509-84905940 | Common:1; Rare:130 | ||||
| chr2:84906114-84906530 | Common:2; Rare:104 | ||||
| chr2:85354517-85354799 | Common:1; Rare:93 | ||||
| chr2:85539072-85539168 | Common:1; Rare:36 | ||||
| chr2:85561424-85561550 | Rare:48; Clinvar:4 |