chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4140564983140564984GA47GENICpossibly homozygous793688872
4140565941140565942GA47GENICheterozygous793688873
4140565949140565950GA47GENICheterozygous793688874
4140567416140567417TA40GENIChomozygous793688875
4140567719140567720GA48GENIChomozygous793688876
4140568687140568688CT29GENIChomozygous793688877
4140568993140568994AG66GENIChomozygous793688878
4140569239140569240AT28GENIChomozygous793688879
4140570080140570081TG31GENIChomozygous793688880
4140570084140570085AG31GENIChomozygous793688881
4140572950140572951AG29GENIChomozygous793688882
4140573002140573003AG46GENIChomozygous793688883
4140573909140573910GC36GENIChomozygous793688884
4140573928140573929CT40GENIChomozygous793688885
4140574076140574077AG34GENIChomozygous793688886
4140574078140574079GA35GENIChomozygous793688887
4140574272140574273CT26GENICpossibly homozygous793688888
4140574548140574549GA44GENIChomozygous793688889
4140574608140574609CT41GENIChomozygous793688890
4140574770140574771AG49GENIChomozygous793688891
4140575255140575256GA56GENIChomozygous793688892
4140575893140575894TG33GENIChomozygous793688893
4140576235140576236TA45GENIChomozygous793688894
4140578417140578418GA45GENIChomozygous793688895
4140593585140593586CA65INTERGENICpossibly homozygous793688896
4140593636140593637AT53INTERGENIChomozygous793688897
4140593642140593643CT49INTERGENIChomozygous793688898