| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74507648-74507785 | Rare:32 | ||||
| chr2:74527625-74527754 | Common:1; Rare:44 | ||||
| chr2:74529623-74530041 | Rare:136; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74958587-74959095 | Common:4; Rare:202 | ||||
| chr2:75560900-75561058 | Rare:35 | ||||
| chr2:75647003-75647152 | Common:1; Rare:36 | ||||
| chr2:75710602-75710802 | Common:2; Rare:82 | ||||
| chr2:75710864-75711328 | Common:2; Rare:119 | ||||
| chr2:84459172-84459615 | Common:3; Rare:120; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84904949-84905350 | Common:2; Rare:83 | ||||
| chr2:84905462-84905949 | Common:2; Rare:146 | ||||
| chr2:84970710-84970819 | Rare:33 | ||||
| chr2:84970939-84971454 | Common:3; Rare:148 | ||||
| chr2:85327916-85328083 | Common:2; Rare:75 | ||||
| chr2:85354501-85354838 | Common:2; Rare:114 |