chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
92178749421787495CG14GENIChomozygous138539676
92178773021787731TA16GENIChomozygous138539677
92178854821788549GC10GENIChomozygous138539678
92178875921788759A16GENIChomozygous142110814
92178990721789909CT15GENIChomozygous138452533
92179094421790945T12GENIChomozygous142110815
92179094621790955CTCCCCTCT12GENIChomozygous142110816
92178881121788812GA19GENIChomozygous142137258
92179095421790955TC12GENICheterozygous403260917
92179094421790945TC12GENICheterozygous403260915
92179095421790955T12GENIChomozygous403260916
92178907221789073AG17GENIChomozygous142137259
92179185421791855TC16GENIChomozygous138539682
92179198121791982TC13GENIChomozygous142137260
92179292021792921GA14GENIChomozygous138539683
92179339321793393TTCT8GENIChomozygous142110817
92179730621797307AG23GENIChomozygous138539690
92179832021798321AG18GENIChomozygous142137261
92179835621798357TC17GENIChomozygous138539693
92180086221800863AG13GENIChomozygous138539698
92180196621801967AG21GENIChomozygous138539706
92180300821803009GC19GENIChomozygous138539707
92180389421803895A6GENICheterozygous403260918
92180389421803895AT6GENICheterozygous403260919
92180417421804175GA20GENIChomozygous142137262
92180482921804830T14GENIChomozygous138452538
92180543221805433AG11GENIChomozygous142137263
92180791321807914CT13GENIChomozygous142137264
92181047121810471T17GENIChomozygous142110818
92181073921810740CG8GENICheterozygous138539724
92181156421811565A22GENIChomozygous142110819
92181194921811950T20GENIChomozygous138452541
92181282421812825A19GENIChomozygous138452542
92181318321813184AG17GENIChomozygous138539727
92181367421813674G22GENIChomozygous142110820
92181506921815070TA13GENIChomozygous138539730
92181519821815199TC15GENIChomozygous142137265
92181540021815401AG21GENIChomozygous138539733
92181561421815615AC5GENIChomozygous142137266
92181564621815647C9GENIChomozygous144399784