| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74178784-74179012 | Common:2; Rare:62 | ||||
| chr2:74421596-74421759 | Rare:55 | ||||
| chr2:74440419-74440673 | Rare:68 | ||||
| chr2:74458128-74458509 | Common:1; Rare:117 | ||||
| chr2:74459680-74459941 | Rare:93 | ||||
| chr2:74482990-74483119 | Rare:55 | ||||
| chr2:74507304-74507587 | Rare:81 | ||||
| chr2:74507669-74507789 | Rare:25 | ||||
| chr2:74529578-74529974 | Rare:133; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:74554646-74554757 | Common:1; Rare:46 | ||||
| chr2:74958876-74959071 | Rare:70 | ||||
| chr2:75710669-75710761 | Common:1; Rare:38 | ||||
| chr2:84459226-84459581 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84905482-84905718 | Common:2; Rare:74 | ||||
| chr2:85327916-85328050 | Common:1; Rare:62 |