chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14160846241608463CT32GENICheterozygous108090612
14160859541608596GT32GENICpossibly homozygous108090613
14160861741608618CT28GENICheterozygous108090614
14160876041608761GA31GENIChomozygous108090615
14160876241608763GC30GENIChomozygous108090616
14160876841608769AG34GENIChomozygous108090617
14164428441644285GA28GENIChomozygous108090618
14164428641644287GC28GENIChomozygous108090619
14164428841644289GC28GENIChomozygous108090620
14164428941644290GC28GENIChomozygous108090621
14164429041644291GA28GENIChomozygous108090622
14167503841675039GA35GENIChomozygous108090623
14167527141675272GT15GENIChomozygous108090624
14167532141675322GC19GENIChomozygous108090625
14167535041675351CA22GENIChomozygous108090626
14168492141684922TA66GENIChomozygous108090627
14168774841687749CT10GENIChomozygous108090628
14168784541687846CT7GENIChomozygous108090629
14173659441736595AG10GENIChomozygous108090630
14174236441742365GA7GENIChomozygous108090631
14174237541742376TA12GENIChomozygous108090632
14174238741742388TA13GENIChomozygous108090633
14174239041742391TA14GENIChomozygous108090634
14174709141747092GT46GENIChomozygous108090635