| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:88554097-88554289 | Rare:38 | ||||
| chr14:88554472-88555078 | Common:7; Rare:170 | ||||
| chr14:88562867-88563280 | Rare:168 | ||||
| chr14:88563322-88563601 | Rare:106 | ||||
| chr14:88792723-88793099 | Common:1; Rare:105 | ||||
| chr14:88824301-88824723 | Common:2; Rare:121; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:88824812-88824996 | Common:1; Rare:42 | ||||
| chr14:88825234-88825323 | Rare:16 | ||||
| chr14:89416364-89416642 | Common:1; Rare:67 | ||||
| chr14:89417059-89417536 | Common:3; Rare:134 | ||||
| chr14:89417539-89417686 | Common:2; Rare:38 | ||||
| chr14:89619106-89619321 | Common:1; Rare:75 | ||||
| chr14:89954491-89954532 | Rare:13 | ||||
| chr14:89954548-89954978 | Common:3; Rare:146 | ||||
| chr14:89955744-89956114 | Common:13; Rare:124; Clinvar:3; Clinvar (benign):1 |