chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1269318706931871GA50GENIChomozygous115359887
1269327756932776GA29GENIChomozygous115359888
1269328426932843GT26GENIChomozygous115359889
1269332736933274GC33GENIChomozygous115359890
1269337996933800TC34GENICheterozygous118321622
1269341376934138CT32GENICpossibly homozygous115436874
1269342346934235GA24GENIChomozygous115359891
1269343766934377GC24GENIChomozygous115444830
1269343876934388CA31GENIChomozygous115444832
1269344356934436CA33GENIChomozygous115359892
1269366856936686TC8GENICheterozygous118321624
1269366896936690TC6GENICheterozygous118321625
1269377816937782GT43GENIChomozygous115359893
1269394566939457AT25GENICpossibly homozygous118321627
1269394586939459AT22GENIChomozygous118321629
1269394606939461AT23GENIChomozygous118321631
1269405186940519TC38GENIChomozygous115359894
1269418716941872GA35GENICheterozygous118321633
1269419306941931CG40GENICheterozygous118242628
1269419336941934CT36GENICheterozygous118242629
1269419346941935TG36GENICheterozygous118321635
1269443256944326CG17GENIChomozygous115359895
1269447486944749GA41GENIChomozygous115359896
1269459036945904AG6GENIChomozygous115504844
1269459086945909CT5GENIChomozygous115436875
1269463406946341AG40GENIChomozygous115359897
1269481596948160AG28GENICpossibly homozygous115436876
1269483726948373CG20GENIChomozygous118321639
1269484086948409GT17GENICheterozygous118321641
1269486496948650GT18GENICheterozygous118335498
1269487346948735TG53GENICheterozygous118321643
1269487516948752GT54GENICheterozygous118321645
1269488256948826GT39GENICpossibly homozygous118321649
1269488606948861GA40GENICpossibly homozygous118321651
1269494016949402GA45GENIChomozygous115359898
1269506296950630TA27GENIChomozygous115359899
1269508306950831AC28GENIChomozygous115359900
1269522666952267CT33GENIChomozygous115359901
1269531796953180GC19GENIChomozygous115359902
1269556976955698TC19GENIChomozygous115359903