| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:88824325-88824721 | Common:2; Rare:115; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89351454-89351631 | Rare:36 | ||||
| chr14:89416601-89416635 | Rare:7 | ||||
| chr14:89417161-89417361 | Rare:49 | ||||
| chr14:89618913-89618995 | Rare:14 | ||||
| chr14:89619122-89619309 | Rare:68 | ||||
| chr14:89954607-89954972 | Common:3; Rare:118 | ||||
| chr14:89955741-89956115 | Common:13; Rare:124; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89956449-89956599 | Common:4; Rare:34; Clinvar (benign):3 | ||||
| chr14:90256451-90256686 | Common:3; Rare:70 | ||||
| chr14:90256953-90257036 | Rare:16 | ||||
| chr14:90257042-90257075 | Rare:7 | ||||
| chr14:90331612-90331770 | Rare:42 | ||||
| chr14:90331855-90332438 | Common:1; Rare:153 | ||||
| chr14:90396786-90397237 | Common:7; Rare:213; Clinvar (benign):2 |