chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107563399575633996TC16GENIChomozygous116639545
107563432475634325AG10GENIChomozygous116639547
107563513175635132TC14GENIChomozygous116639555
107563543175635432TC16GENIChomozygous116639563
107563585275635853GA8GENIChomozygous116800576
107563601175636012CT14GENIChomozygous116800578
107563662875636629TA11GENIChomozygous116639571
107563899475638995TC27GENIChomozygous116639591
107563901175639012AC23GENIChomozygous116639593
107563971475639715AG10GENIChomozygous116639595
107564073275640733GA18GENIChomozygous116800580
107564133575641336TC19GENIChomozygous116800582
107564273175642732AC12GENIChomozygous116639621
107564285975642860AG5GENIChomozygous116800584
107564298775642988TC20GENICpossibly homozygous116639623