chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10103396129103396130AG5GENIChomozygous116832760
10103396908103396909GT9GENIChomozygous116832762
10103396963103396964AG7GENIChomozygous116832764
10103397840103397841AC9GENIChomozygous116832766
10103398412103398413TA10GENIChomozygous116832768
10103398831103398832TC11GENIChomozygous116832770
10103399605103399606CT16GENIChomozygous116832772
10103399640103399641CT18GENIChomozygous116832774
10103399708103399709CT6GENIChomozygous116832776
10103400050103400051TC3GENIChomozygous116832778
10103400064103400065GT4GENIChomozygous116832780
10103400170103400171GA9GENIChomozygous116832782
10103400402103400403CT8GENIChomozygous116832784
10103404264103404265AC6GENIChomozygous116832786
10103404935103404936GC6GENIChomozygous116832788
10103405094103405095AG10GENIChomozygous116832790
10103405143103405144CA6GENIChomozygous116832792
10103405188103405189CT12GENIChomozygous116832794
10103405237103405238TC13GENIChomozygous116832796
10103405245103405246TC14GENIChomozygous116832798
10103405476103405477AG8GENIChomozygous116832800
10103407080103407081GA8GENIChomozygous116832802
10103411551103411552CT8GENIChomozygous116832804
10103412475103412476TA2GENIChomozygous116832806
10103412481103412482TG2GENIChomozygous116832808
10103412485103412486TA2GENIChomozygous116832809
10103413918103413919TC13GENIChomozygous116832811
10103415005103415006TC3GENIChomozygous116832813
10103416073103416074TC15GENIChomozygous116832815
10103416287103416288TC9GENIChomozygous116832817
10103416585103416586CT6GENIChomozygous116832819
10103416847103416848TC7GENIChomozygous116832821
10103416956103416957TC11GENIChomozygous116832823
10103416976103416977GA10GENIChomozygous116832825
10103417037103417038GA8GENIChomozygous116832827
10103417067103417068GA10GENIChomozygous116832829