chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4150436018150436019GC12GENIChomozygous112883849
4150438387150438388AG32GENIChomozygous112883851
4150446817150446818CA25GENIChomozygous113182006
4150449012150449013CG21GENIChomozygous112883873
4150449049150449050GA20GENIChomozygous113182009
4150449329150449330AG28GENIChomozygous112883875
4150449523150449524AG29GENIChomozygous112883876
4150454318150454319TA19GENIChomozygous113182012
4150454153150454154AG15GENIChomozygous113182010
4150454295150454296GA20GENIChomozygous113182011
4150454327150454328TA15GENIChomozygous113182013
4150455382150455383TA26GENIChomozygous113182014
4150455555150455556AG20GENICpossibly homozygous112883885
4150456742150456743CT25GENIChomozygous112883886
4150457329150457330GA19GENIChomozygous112883887
4150458645150458646CT34GENIChomozygous113182015
4150459894150459895CT22GENIChomozygous112883890
4150460358150460359TC29GENIChomozygous112883891
4150460744150460745CT15GENIChomozygous112883893
4150460716150460717GA14GENIChomozygous112883892
4150462484150462485TC33GENIChomozygous112883894
4150464813150464814CT25GENIChomozygous113182016
4150467066150467067AG25GENIChomozygous112883897
4150467070150467071GA28GENIChomozygous112883898
4150467092150467093AG29GENIChomozygous112883899
4150467150150467151GA26GENIChomozygous112883900
4150467929150467930AG10GENIChomozygous112883901
4150467998150467999AG7GENIChomozygous112883902
4150468592150468593GA28GENIChomozygous113182018
4150469828150469829AG21GENIChomozygous113182019
4150471224150471225TA32GENIChomozygous112883907
4150471493150471494CG28GENIChomozygous113182020
4150471579150471580CG13GENIChomozygous113182021