| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:60249632-60249948 | Common:2; Rare:88 | ||||
| chr14:60485605-60485848 | Common:2; Rare:59 | ||||
| chr14:60485929-60486203 | Common:2; Rare:75 | ||||
| chr14:60508959-60509173 | Rare:40 | ||||
| chr14:60514816-60515094 | Common:1; Rare:85 | ||||
| chr14:60515106-60515213 | Common:1; Rare:27 | ||||
| chr14:60648913-60649149 | Rare:65; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:60649399-60649712 | Common:3; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:60723333-60723472 | Rare:43 | ||||
| chr14:60724292-60724369 | Common:1; Rare:22 | ||||
| chr14:60734690-60734868 | Rare:63 | ||||
| chr14:60980803-60980894 | Rare:32 | ||||
| chr14:60980972-60981321 | Common:1; Rare:133 | ||||
| chr14:60981442-60981724 | Rare:80 | ||||
| chr14:60982147-60982257 | Rare:31 |