chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107424117974241180CT33GENICheterozygous116636663
107424131874241319GT84GENICheterozygous116636667
107424173074241731AG63GENICheterozygous116636671
107424187174241872CG50GENICheterozygous116636675
107424242874242429GT20GENICheterozygous117197182
107424253874242539GT82GENICheterozygous116636677
107424265674242657GC125GENICheterozygous116636679
107424265974242660GT128GENICheterozygous116636681
107424293874242939CT49GENICheterozygous117257087
107424336374243364CA86GENICheterozygous116636687
107424372974243730GA81GENICheterozygous116636693
107424373274243733CT78GENICheterozygous116636695
107424373374243734GC78GENICheterozygous116636697
107424396374243964AG66GENICheterozygous116636699
107424408674244087TC57GENICheterozygous116636703
107424410774244108CG54GENICheterozygous116636705
107424418974244190GA52GENICheterozygous116636709
107424420174244202GA50GENICheterozygous116636711
107424444174244442GT67GENICheterozygous116636715
107424449874244499GC65GENICheterozygous116636717
107424456274244563GT62GENICheterozygous116636719
107424486774244868CT70GENICheterozygous116636721
107424498274244983AG99GENICheterozygous116636723
107424504174245042GC104GENICheterozygous116636725
107424443974244440CA67GENICheterozygous116800144
107424518374245184TC139GENICheterozygous116636727
107424591474245915TC15GENIChomozygous117257089
107424691474246915CT17GENIChomozygous117064320
107424747374247474TC41GENIChomozygous116636731
107424751774247518CG36GENIChomozygous116636733
107424793874247939CT64GENIChomozygous116636739
107424801174248012AG32GENIChomozygous116636741
107424938974249390CG55GENICheterozygous116636745
107427746174277462CT115GENICheterozygous116636837
107427748574277486CA122GENICheterozygous116636838
107427755574277556GA128GENICheterozygous116636840
107424686274246863GT24GENIChomozygous117278393
107424619174246192GA21GENICheterozygous117278389
107424620174246202AG21GENICheterozygous117278391