| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:52951003-52951461 | Common:4; Rare:165 | ||||
| chr14:53152371-53152534 | Rare:61; Clinvar (benign):1 | ||||
| chr14:53153288-53153409 | Common:1; Rare:52 | ||||
| chr14:53953380-53953639 | Common:2; Rare:74 | ||||
| chr14:53956734-53956986 | Rare:59; Clinvar:1 | ||||
| chr14:54488830-54489164 | Common:3; Rare:96 | ||||
| chr14:54567453-54567503 | Rare:6 | ||||
| chr14:54902824-54902935 | Rare:28; Clinvar (benign):1 | ||||
| chr14:55027046-55027359 | Common:2; Rare:82 | ||||
| chr14:55051473-55051802 | Common:1; Rare:147 | ||||
| chr14:55129086-55129298 | Common:1; Rare:58 | ||||
| chr14:55191502-55191756 | Common:5; Rare:57 | ||||
| chr14:55271245-55271491 | Common:2; Rare:86 | ||||
| chr14:55272076-55272287 | Common:1; Rare:48 | ||||
| chr14:55411731-55411905 | Common:1; Rare:84 |