chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142410380024103801TG17INTERGENIChomozygous813690083
142410385924103860TA14INTERGENIChomozygous813690084
142410427124104272TC20GENIChomozygous813690085
142410436724104368TC19GENIChomozygous813690086
142410441624104417GC19GENIChomozygous813690087
142410456424104565GA14GENIChomozygous813690088
142410471824104719GA16GENIChomozygous813690089
142410474224104743TC12GENIChomozygous813690090
142410666324106664AG6GENIChomozygous813690091
142410669524106696GA10GENIChomozygous813690092
142410741224107413AG19GENIChomozygous813690093
142410823824108239CT8GENIChomozygous813690094
142410841524108416TC17GENIChomozygous813690095
142410844724108448TC10GENIChomozygous813690096
142410961424109615TC27GENIChomozygous813690097
142410964224109643CT21GENIChomozygous813690098
142410982324109824GT19GENIChomozygous813690099
142410989424109895GT14GENIChomozygous813690100
142410999024109991GC16GENIChomozygous813690101
142411021424110215GA2GENIChomozygous813690102
142411603824116039GT16GENIChomozygous813690103
142411609024116091CG22GENIChomozygous813690104
142411653724116538TC15GENIChomozygous813690105
142411671024116711GA8GENIChomozygous813690106
142411704524117046AC11GENIChomozygous813690107
142411751424117515CT16GENICheterozygous813690108
142411943824119439TA17GENIChomozygous813690109
142411988824119889GA29GENIChomozygous813690110
142412028624120287GA5GENIChomozygous813690111
142412123724121238GA18GENIChomozygous813690112
142412148724121488GA11GENIChomozygous813690113
142412186924121870AT24GENIChomozygous813690114
142412243424122435AG25GENIChomozygous813690115
142412329224123293GT22GENIChomozygous813690116
142412331324123314GC19GENIChomozygous813690117
142412389124123892GC19GENIChomozygous813690118
142412462824124629AG5GENIChomozygous813690119
142412524224125243TC15GENIChomozygous813690120