| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:64502816-64503375 | Common:8; Rare:391 | ||||
| chr14:64503430-64504430 | Common:24; Rare:1143 | ||||
| chr14:64504361-64504930 | Common:8; Rare:747 | ||||
| chr14:64505046-64505788 | Common:19; Rare:603 | ||||
| chr14:64879820-64880738 | Common:15; Rare:443 | ||||
| chr14:64914060-64914530 | Common:5; Rare:306 | ||||
| chr14:64914454-64915080 | Common:6; Rare:225 | ||||
| chr14:64986590-64986932 | Common:3; Rare:233 | ||||
| chr14:64986878-64987367 | Rare:809 | ||||
| chr14:65102081-65103027 | Common:61; Rare:1125; Clinvar:19; Clinvar (benign):31 | ||||
| chr14:65103076-65103476 | Common:4; Rare:102 | ||||
| chr14:65411601-65412001 | Common:7; Rare:198 | ||||
| chr14:65412250-65413080 | Common:27; Rare:833 | ||||
| chr14:65413362-65414090 | Common:8; Rare:305 | ||||
| chr14:66507263-66507665 | Common:2; Rare:151 |