chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2202471334202471335AT18GENIChomozygous111002721
2202471535202471536AC22GENICpossibly homozygous111002723
2202472881202472882AG14GENIChomozygous111002725
2202473195202473196GC26GENIChomozygous111002727
2202473214202473215AG25GENIChomozygous111002729
2202473256202473257AG23GENIChomozygous111002731
2202474394202474395AC25GENIChomozygous111002733
2202474483202474484AG20GENIChomozygous111002735
2202475026202475027GA24GENIChomozygous111002737
2202475074202475075TC24GENIChomozygous111002739
2202475498202475499CT15GENIChomozygous111002741
2202475755202475756AG14GENIChomozygous111002743
2202475760202475761CT17GENIChomozygous110208419
2202475826202475827CT18GENIChomozygous111002745
2202476422202476423AG29GENIChomozygous110208422
2202476560202476561TC27GENICpossibly homozygous111002747
2202478818202478819CT25GENIChomozygous111002749
2202479617202479618TC14GENIChomozygous110208423
2202479943202479944TA10GENIChomozygous111002751
2202480942202480943GA12GENICpossibly homozygous111002753
2202481281202481282CA12GENIChomozygous110208424
2202481672202481673AC18GENIChomozygous110208426
2202483067202483068AG24GENIChomozygous110208427
2202483424202483425GA21GENIChomozygous111002755
2202485204202485205TA31GENIChomozygous111002757
2202490610202490611AC6GENIChomozygous110208448
2202491903202491904GC14GENIChomozygous110208452
2202496142202496143GA18GENIChomozygous110208460
2202504695202504696GA6GENIChomozygous111002759
2202505372202505373TG22GENIChomozygous110208466
2202505995202505996CA18GENIChomozygous111002761
2202509066202509067AG19GENIChomozygous110208469
2202511268202511269TC15GENIChomozygous110208472
2202513922202513923GA27GENIChomozygous111002763
2202521180202521181AT5GENIChomozygous111002765
2202522481202522482AG37GENIChomozygous110208491
2202522597202522598AC27GENIChomozygous110208492
2202523710202523711GA38GENIChomozygous111002769
2202525138202525139AG32GENIChomozygous110208496