chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242322324232233TC18GENIChomozygous50002798
1242327264232727AG29GENIChomozygous50002799
1242328904232891TTCCCTCC9GENIChomozygous50002800
1242336644233670GTGTGT------7GENICpossibly homozygous50002801
1242338354233836GC18GENIChomozygous50002802
1242338884233889GA16GENIChomozygous50002803
1242340884234089TC20GENIChomozygous50002804
1242343054234306TC19GENIChomozygous50002805
1242344524234453TC19GENIChomozygous50002806
1242346594234660A-17GENICpossibly homozygous50002807
1242346604234665AACAC-----19GENICheterozygous50002808
1242348524234867AAAAAAAGAAAGAAA---------------5GENICheterozygous50002809
1242350874235088TG26GENIChomozygous50002810
1242355454235546GC25GENICpossibly homozygous50002811
1242358524235853CA19GENIChomozygous50002812
1242359274235928TC29GENICpossibly homozygous50002813
1242359854235986TC29GENICpossibly homozygous50002814
1242373164237317GT17GENIChomozygous50002815
1242374124237413TTGGTTATTCAACTCGACCTTTGAA10GENIChomozygous50002816
1242374454237446AAT26GENIChomozygous50002817
1242374524237453GA28GENIChomozygous50002818
1242396454239646TA25GENIChomozygous50002819
1242401504240151CCT24GENIChomozygous50002820
1242415534241557GTGT----4GENIChomozygous50274556
1242430874243091GTGT----13GENIChomozygous50416967
1242440344244035TTTC9GENICheterozygous50002823
1242440824244083AAGTGTGT3GENIChomozygous50274558
1242454294245430GGAC23GENIChomozygous50458420
1242455704245571TTAC36GENIChomozygous50002826
1242484834248484CA5GENIChomozygous50002828
1242491914249193AA--17GENICheterozygous50002829
1242519794251980AG30GENIChomozygous50002830
1242541964254197AG27GENICpossibly homozygous50458422
1242547054254709TACA----15GENIChomozygous50394265
1242586264258627CT21GENIChomozygous50458424