| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:45135680-45136485 | Common:5; Rare:550; Clinvar:19; Clinvar (benign):4 | ||||
| chr14:45251975-45252705 | Common:2; Rare:167 | ||||
| chr14:45253045-45253496 | Common:1; Rare:237 | ||||
| chr14:49586293-49586714 | Common:7; Rare:963; Clinvar (benign):2 | ||||
| chr14:49598293-49598567 | Rare:73 | ||||
| chr14:49598500-49599080 | Common:16; Rare:948 | ||||
| chr14:49599100-49599430 | Rare:311 | ||||
| chr14:49599431-49599831 | Common:4; Rare:88 | ||||
| chr14:49600065-49600465 | Common:1; Rare:104 | ||||
| chr14:49620158-49620558 | Common:1; Rare:122 | ||||
| chr14:49620487-49620912 | Common:16; Rare:832; Clinvar:23 | ||||
| chr14:49620923-49621452 | Common:2; Rare:380; Clinvar:10; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr14:49634697-49635493 | Common:13; Rare:492; Clinvar:15; Clinvar (benign):19; Clinvar (pathogenic):4 | ||||
| chr14:49635558-49635958 | Common:7; Rare:62 | ||||
| chr14:49688036-49688815 | Common:10; Rare:538 |