chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152754309727543098CT38GENIChomozygous48482694
152754418927544190GA46GENIChomozygous48482696
152754507327545074AG21GENIChomozygous48482698
152754638127546382GA29GENIChomozygous48482700
152754653827546539CT28GENIChomozygous48482702
152754848627548487AG26GENIChomozygous48482704
152754909127549092AG43GENIChomozygous48482706
152754940727549408TC30GENIChomozygous48482708
152754976227549763GA24GENIChomozygous48482710
152754991427549915GA36GENIChomozygous48482712
152755019727550198TC23GENIChomozygous48482714
152755037727550378TTGAG36GENIChomozygous48482716
152755067327550674TTAA22GENIChomozygous48482718
152755102627551027CCAA12GENICheterozygous48482722
152755102627551027CCA12GENICheterozygous48482724
152755105727551058A-16GENICpossibly homozygous48482726
152755109427551217CTGAGCAGGGAATTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC---------------------------------------------------------------------------------------------------------------------------22GENICpossibly homozygous49042323
152755179027551791GA32GENIChomozygous48482728
152755253827552539AG37GENIChomozygous48482730
152755306527553066T-8GENICpossibly homozygous48482732
152755306527553072TCTCTCT-------8GENICheterozygous49042327
152755306727553072TCTCT-----8GENICpossibly homozygous48482734
152755380327553804TTA21GENIChomozygous48482737
152755415127554152CG11GENIChomozygous48482739
152755442827554429TC13GENIChomozygous48482741
152755448127554487CGCGGA------1GENIChomozygous48482744
152755474227554743AT26GENIChomozygous48482746
152755291127552912GA38GENIChomozygous49359076
152755381427553815CA28GENIChomozygous49359077