| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74465314-74465547 | Common:2; Rare:64; Clinvar:1 | ||||
| chr2:74482738-74483134 | Common:1; Rare:141 | ||||
| chr2:74502500-74502670 | Rare:48 | ||||
| chr2:74503307-74503468 | Rare:40 | ||||
| chr2:74507351-74507602 | Rare:71 | ||||
| chr2:74507669-74507985 | Common:2; Rare:80 | ||||
| chr2:74529607-74530013 | Rare:134; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74654134-74654285 | Rare:41 | ||||
| chr2:74958332-74958782 | Common:7; Rare:152 | ||||
| chr2:74958850-74959046 | Rare:72 | ||||
| chr2:75710658-75710778 | Common:2; Rare:47 | ||||
| chr2:84459180-84459593 | Common:3; Rare:110; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84881030-84881215 | Common:1; Rare:52 | ||||
| chr2:84906579-84906894 | Common:4; Rare:48 | ||||
| chr2:84970648-84970966 | Common:2; Rare:106 |