| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:52791423-52791764 | Common:1; Rare:113 | ||||
| chr14:52864558-52864810 | Common:1; Rare:71 | ||||
| chr14:53152264-53152529 | Rare:97; Clinvar (benign):2 | ||||
| chr14:53953439-53953608 | Common:2; Rare:48 | ||||
| chr14:54488901-54489132 | Common:1; Rare:68 | ||||
| chr14:54566990-54567199 | Rare:52 | ||||
| chr14:54652197-54652553 | Rare:54 | ||||
| chr14:55027035-55027451 | Common:4; Rare:99 | ||||
| chr14:55051470-55051803 | Common:1; Rare:148 | ||||
| chr14:55137240-55137394 | Common:1; Rare:32 | ||||
| chr14:55191518-55191750 | Common:5; Rare:53 | ||||
| chr14:55411603-55411729 | Common:1; Rare:42 | ||||
| chr14:55411785-55411952 | Common:2; Rare:82 | ||||
| chr14:55580059-55580351 | Common:3; Rare:118 | ||||
| chr14:55672625-55673333 | Common:3; Rare:198 |