| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35122158-35122801 | Common:6; Rare:484 | ||||
| chr14:35292119-35292620 | Common:15; Rare:376; Clinvar:2 | ||||
| chr14:35403673-35404273 | Common:5; Rare:429; Clinvar:2; Clinvar (benign):5 | ||||
| chr14:35404540-35404966 | Common:8; Rare:355; Clinvar:3; Clinvar (benign):10 | ||||
| chr14:35405060-35405250 | Common:1; Rare:66 | ||||
| chr14:35533849-35534096 | Rare:72 | ||||
| chr14:35808530-35808860 | Common:2; Rare:100 | ||||
| chr14:35808847-35809020 | Rare:43 | ||||
| chr14:35809173-35809387 | Common:2; Rare:94 | ||||
| chr14:35826042-35826535 | Common:2; Rare:313 | ||||
| chr14:35826608-35826783 | Rare:62 | ||||
| chr14:35826686-35826960 | Common:2; Rare:141 | ||||
| chr14:36320083-36320189 | Rare:15 | ||||
| chr14:36320518-36320834 | Common:9; Rare:218 | ||||
| chr14:36520084-36520379 | Common:1; Rare:95; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 |