chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
79976788799767888TTGGG1GENIChomozygous740790500
79976788999767890AG1GENIChomozygous625370470
79976839999768400AT1GENIChomozygous625370471
79976916799769170GAG---10GENICheterozygous740790501
79977005999770060TC5GENIChomozygous625370472
79977016899770169TC1GENIChomozygous625370473
79977113199771132TG16GENIChomozygous625370474
79977115799771158AT24GENICpossibly homozygous625370475
79977166099771661GA23GENICpossibly homozygous625370476
79977343299773433TC9GENIChomozygous625370477
79977444699774447TC6GENIChomozygous625370478
79977447299774473GT6GENICheterozygous625370479
79977483699774837TC9GENIChomozygous625370480
79977485299774853TC11GENIChomozygous625370481
79977496199774962AG10GENIChomozygous625370482
79977516499775165AG11GENICheterozygous625370483
79977541299775413TG3GENICheterozygous625370484
79977657999776580GT17GENICpossibly homozygous625370485