chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152754309727543098CT23GENIChomozygous48482694
152754418927544190GA11GENIChomozygous48482696
152754507327545074AG17GENIChomozygous48482698
152754638127546382GA31GENIChomozygous48482700
152754653827546539CT24GENIChomozygous48482702
152754848627548487AG22GENIChomozygous48482704
152754909127549092AG12GENIChomozygous48482706
152754940727549408TC14GENIChomozygous48482708
152754976227549763GA24GENIChomozygous48482710
152754991427549915GA29GENIChomozygous48482712
152755019727550198TC12GENIChomozygous48482714
152755037727550378TTGAG20GENIChomozygous48482716
152755067327550674TTAA15GENIChomozygous48482718
152755083327550834GGC8GENICheterozygous48744221
152755102627551027CCAA13GENICheterozygous48482722
152755102627551027CCA13GENICheterozygous48482724
152755105727551058A-11GENIChomozygous48482726
152755109427551217CTGAGCAGGGAATTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC---------------------------------------------------------------------------------------------------------------------------18GENIChomozygous49042323
152755129827551299AACC14GENIChomozygous48815719
152755179027551791GA8GENIChomozygous48482728
152755253827552539AG27GENIChomozygous48482730
152755290327552904TC13GENIChomozygous48815721
152755306227553086CTCTCTCTCTCCCTCCCTCCCTCC------------------------17GENICpossibly homozygous49436998
152755321027553211CT29GENIChomozygous48815723
152755380427553806AA--22GENIChomozygous48744233
152755403227554033AG17GENIChomozygous48744235
152755442827554429TC26GENIChomozygous48482741
152755448127554487CGCGGA------21GENIChomozygous48482744
152755474227554743AT30GENIChomozygous48482746