| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75427643-75427727 | Rare:22 | ||||
| chr14:75660813-75661334 | Common:4; Rare:124 | ||||
| chr14:75985714-75985789 | Rare:32; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr14:76812837-76813019 | Common:2; Rare:64 | ||||
| chr14:76826244-76826404 | Common:1; Rare:20 | ||||
| chr14:77028284-77028557 | Common:5; Rare:77 | ||||
| chr14:77098001-77098348 | Rare:107 | ||||
| chr14:77320838-77321105 | Rare:82; Clinvar:1 | ||||
| chr14:77377022-77377415 | Common:3; Rare:117 | ||||
| chr14:77457529-77457876 | Common:1; Rare:106 | ||||
| chr14:77457966-77458151 | Rare:53 | ||||
| chr14:77616583-77616738 | Common:2; Rare:58; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:77707991-77708126 | Rare:67 | ||||
| chr14:81220867-81221069 | Common:1; Rare:95 | ||||
| chr14:81221288-81221423 | Common:1; Rare:31 |