chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185630612756306128AG21GENIChomozygous110543163
185630622856306229CT38GENIChomozygous110543165
185630630356306304GA27GENIChomozygous110543167
185630803256308033AT14GENIChomozygous110919607
185630820556308206GT19GENIChomozygous110543169
185630913756309138CT7GENIChomozygous110543171
185630939156309392TC16GENIChomozygous110361353
185630996056309961GA17GENIChomozygous110543173
185631052856310529GA23GENIChomozygous110361357
185631205256312053AG18GENIChomozygous110361361
185631334956313350GA20GENIChomozygous110361367
185631361256313613GA12GENIChomozygous110361369
185631424756314248AG18GENIChomozygous110361371
185631474656314747CT12GENIChomozygous110361373
185631530756315308TC23GENIChomozygous110361375
185631554956315550CT18GENIChomozygous110543180
185631557956315580GA20GENIChomozygous110361377
185631579456315795CT16GENIChomozygous110361379
185631587356315874CT26GENIChomozygous110361381
185631648956316490AC21GENIChomozygous110361383
185631671156316712CT26GENIChomozygous110361385
185631992956319930AG17GENIChomozygous125353055
185632057156320572AG25GENIChomozygous125353057
185632260556322606TC18GENIChomozygous125353073
185632263356322634AT17GENIChomozygous125390792
185631738556317386AG5GENIChomozygous125403434
185631872356318724CT15GENIChomozygous125403436
185631901556319016GA8GENIChomozygous125390790
185632133556321336CG30GENIChomozygous125390791