chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13632097236320973GC53GENIChomozygous108076076
13632160536321606CT39GENIChomozygous108076083
13632263136322632TA18GENIChomozygous108076088
13632269636322697AC9GENIChomozygous108076089
13632336836323369TC49GENIChomozygous108076098
13632345736323458AT40GENIChomozygous109475605
13632353436323535TC40GENIChomozygous108076101
13632387436323875TA37GENIChomozygous108076104
13632403336324034CT50GENIChomozygous109475607
13632404336324044GT59GENIChomozygous109475608
13632472436324725TG18GENIChomozygous120471250
13632486336324864CG38GENIChomozygous108076110
13632740536327406GA4GENIChomozygous120500547
13632874836328749TG70GENIChomozygous108076150
13633352836333529TC35GENIChomozygous108076198
13633872036338721AT53GENIChomozygous108076250
13633872136338722AC55GENIChomozygous108076251
13634230636342307CT40GENIChomozygous108076280
13634243036342431TC49GENIChomozygous108076281
13634568836345689AT33GENIChomozygous108076287
13634719636347197AC18GENIChomozygous109475620
13634778136347782GA28GENIChomozygous108076290
13634853636348537TG21GENIChomozygous109475623
13634868436348685CA40GENIChomozygous108076294
13634900236349003TG35GENIChomozygous108076295
13635242436352425TC44GENIChomozygous108076300
13635320836353209AG39GENIChomozygous108076301
13635389336353894CG63GENIChomozygous108076302
13635408536354086TC77GENIChomozygous108076304
13635460036354601CT37GENIChomozygous108076305
13633865736338658GA47GENIChomozygous120554252
13634289536342896GA40GENIChomozygous120554254
13634855236348553AG18GENIChomozygous120554256
13635087936350880AT21GENIChomozygous120554258