| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:71068539-71068634 | Rare:43 | ||||
| chr2:71130225-71130676 | Common:6; Rare:129; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73233183-73233522 | Common:1; Rare:101 | ||||
| chr2:73737304-73737563 | Common:3; Rare:86 | ||||
| chr2:73926696-73926939 | Common:2; Rare:118; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74147872-74148101 | Common:1; Rare:60; Clinvar:2 | ||||
| chr2:74178800-74179022 | Common:2; Rare:63 | ||||
| chr2:74421674-74421759 | Rare:29 | ||||
| chr2:74482928-74483093 | Common:1; Rare:54 | ||||
| chr2:74507652-74507790 | Rare:30 | ||||
| chr2:74529662-74529791 | Rare:51; Clinvar:1 | ||||
| chr2:75561327-75561588 | Common:2; Rare:33 | ||||
| chr2:84459234-84459581 | Common:3; Rare:87; Clinvar:4; Clinvar (benign):4 | ||||
| chr2:84905506-84906117 | Common:2; Rare:171 | ||||
| chr2:85327922-85328080 | Common:2; Rare:73 |