| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49600120-49600293 | Rare:42 | ||||
| chr14:49620191-49620462 | Rare:72 | ||||
| chr14:49620546-49620936 | Common:3; Rare:143; Clinvar:6; Clinvar (benign):1 | ||||
| chr14:49620951-49621329 | Common:1; Rare:120; Clinvar:4; Clinvar (benign):1 | ||||
| chr14:49634577-49634989 | Common:2; Rare:171; Clinvar:16; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr14:49635007-49635577 | Common:5; Rare:136; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr14:49688005-49688054 | Rare:10 | ||||
| chr14:49688075-49688331 | Common:1; Rare:101 | ||||
| chr14:49693016-49693208 | Common:1; Rare:76 | ||||
| chr14:49693362-49693584 | Common:1; Rare:79 | ||||
| chr14:49766927-49767308 | Common:2; Rare:64 | ||||
| chr14:49767443-49767831 | Common:3; Rare:126 | ||||
| chr14:49767918-49768353 | Common:2; Rare:146 | ||||
| chr14:49768368-49768786 | Rare:148 | ||||
| chr14:49768794-49769080 | Rare:57 |