| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:88473551-88474299 | Common:9; Rare:305 | ||||
| chr14:88554647-88555280 | Common:13; Rare:333 | ||||
| chr14:88562847-88563202 | Rare:381 | ||||
| chr14:88563372-88563691 | Rare:269; Clinvar (benign):1 | ||||
| chr14:88792554-88793156 | Common:2; Rare:322 | ||||
| chr14:88824237-88824761 | Common:8; Rare:372; Clinvar:9; Clinvar (benign):3 | ||||
| chr14:89417027-89417414 | Common:3; Rare:256 | ||||
| chr14:89619070-89619310 | Common:1; Rare:83 | ||||
| chr14:89954444-89954968 | Common:9; Rare:465 | ||||
| chr14:89955656-89956143 | Common:31; Rare:326; Clinvar:9; Clinvar (benign):3 | ||||
| chr14:89956335-89956612 | Common:4; Rare:68; Clinvar (benign):3 | ||||
| chr14:90256445-90256672 | Common:5; Rare:124 | ||||
| chr14:90331610-90331770 | Rare:42 | ||||
| chr14:90331860-90332412 | Common:3; Rare:336 | ||||
| chr14:90396781-90397198 | Common:19; Rare:548; Clinvar (benign):1 |