chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42204565722045658AG19GENIChomozygous112543455
42204588322045884CT17GENIChomozygous112543457
42204650122046502TC19GENIChomozygous112543459
42204670222046703GT9GENIChomozygous126004899
42204696422046965GA5GENIChomozygous112543464
42204697222046973AC5GENIChomozygous126039286
42204711622047117TC4GENIChomozygous119376702
42204807422048075GA9GENIChomozygous119303360
42204859022048591GA10GENIChomozygous112543468
42204896622048967TC9GENIChomozygous112543470
42204911522049116AG12GENIChomozygous112543472
42204911922049120TC13GENIChomozygous112543474
42204976122049762GT18GENIChomozygous112543476
42205016322050164TC10GENIChomozygous112543478
42205300222053003CG8GENIChomozygous126004913
42205302122053022CA10GENIChomozygous126004915
42205309722053098GA8GENIChomozygous126039287
42205310522053106GT10GENIChomozygous126039288
42204731722047318AT4GENIChomozygous126086523
42205306722053068GT11GENIChomozygous126046816
42206468422064685TA17GENIChomozygous126004917
42206474422064745TC26GENIChomozygous126004919
42206488822064889GA17GENIChomozygous126004921
42206496122064962CA26GENIChomozygous126004923
42206535222065353AG20GENIChomozygous126004925
42206542822065429AT28GENIChomozygous126004927
42206601422066015GA20GENIChomozygous126004929
42206644822066449TC12GENIChomozygous126004931
42206791722067918CT9GENIChomozygous126004933
42206791922067920TC8GENIChomozygous126004935
42206795022067951AG7GENIChomozygous126004937
42206846922068470AG23GENIChomozygous126004939