| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:54652240-54652690 | Rare:68 | ||||
| chr14:54902119-54902339 | Common:2; Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr14:54902817-54902979 | Rare:46; Clinvar (benign):1 | ||||
| chr14:55026955-55027292 | Common:2; Rare:94 | ||||
| chr14:55027457-55027598 | Rare:25 | ||||
| chr14:55051339-55051671 | Common:1; Rare:108 | ||||
| chr14:55052054-55052345 | Common:2; Rare:78 | ||||
| chr14:55191075-55191345 | Rare:44 | ||||
| chr14:55191518-55191847 | Common:7; Rare:90 | ||||
| chr14:55271199-55271449 | Common:2; Rare:83 | ||||
| chr14:55272053-55272217 | Common:1; Rare:43 | ||||
| chr14:55411792-55411981 | Common:3; Rare:92 | ||||
| chr14:55580073-55580279 | Common:2; Rare:82 | ||||
| chr14:56119176-56119576 | Common:4; Rare:155 | ||||
| chr14:57268313-57268631 | Rare:73 |