chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4100525184100525184A34GENIChomozygous128063691
4100525187100525191CCCC34GENIChomozygous128063692
4100525193100525193G32GENIChomozygous128063693
4100525197100525198GT32GENIChomozygous112798617
4100525199100525200GT34GENIChomozygous112798619
4100525203100525203G35GENIChomozygous128063694
4100528711100528712CA13GENIChomozygous113537732
4100544268100544269T41GENIChomozygous128063695
4100544271100544272TC41GENIChomozygous119279532
4100544333100544334G56GENIChomozygous128063696
4100582563100582563A19GENIChomozygous128063697
4100584271100584271T24GENIChomozygous128063698
4100584304100584305C30GENIChomozygous128063699
4100584341100584342G35GENIChomozygous128063700
4100587411100587411G5GENIChomozygous128063701
4100587567100587567C3GENIChomozygous128063702
4100587572100587573A2GENIChomozygous128063703
4100587575100587575C2GENIChomozygous128063704
4100587687100587687C1GENIChomozygous128063705
4100587723100587723G2GENIChomozygous128063706
4100587738100587738G2GENIChomozygous128063707
4100587751100587752G2GENIChomozygous128063708
4100595617100595618C39GENIChomozygous128063709
4100595620100595622GG39GENIChomozygous128063710
4100595626100595626T38GENIChomozygous128063711
4100595640100595640G39GENIChomozygous128063712
4100595663100595664T36GENIChomozygous128063713
4100608868100608868CTTCCTCCTA46GENIChomozygous128063717
4100612803100612804CT41GENIChomozygous112798625
4100622990100622991TC36GENICheterozygous112798635
4100622993100622994TC37GENICheterozygous112798637
4100622997100622998CA45GENICheterozygous112798639
4100623002100623003AG42GENICheterozygous112798640
4100618218100618219CA26GENICheterozygous130652141
4100634309100634310TC24GENICheterozygous130652142
4100656005100656006CG24GENIChomozygous119279534
4100656007100656016TTAAAAAAA27GENICpossibly homozygous128063718
4100656020100656020ATCATTTTT26GENICheterozygous128063719