| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:88594123-88594460 | Common:1; Rare:56 | ||||
| chr14:88792824-88793029 | Rare:63 | ||||
| chr14:88824337-88824893 | Common:2; Rare:167; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89416944-89417153 | Rare:66 | ||||
| chr14:89619097-89619309 | Common:1; Rare:73 | ||||
| chr14:89952577-89952729 | Common:1; Rare:29 | ||||
| chr14:89954555-89954960 | Common:3; Rare:136 | ||||
| chr14:89955870-89955962 | Common:2; Rare:34; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89957865-89958021 | Common:2; Rare:27 | ||||
| chr14:90061651-90061775 | Common:5; Rare:26 | ||||
| chr14:90256485-90256607 | Common:1; Rare:38 | ||||
| chr14:90331857-90332012 | Common:1; Rare:62 | ||||
| chr14:90332033-90332181 | Rare:32 | ||||
| chr14:90396870-90397192 | Common:5; Rare:152 | ||||
| chr14:90397196-90397232 | Rare:14; Clinvar (benign):1 |