chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3120606088120606089TC61GENIChomozygous58020868
3120606260120606261GT42GENICpossibly homozygous58020870
3120606322120606323TC44GENICpossibly homozygous58020872
3120606357120606358CT49GENIChomozygous58020874
3120607209120607210TC28GENIChomozygous58020876
3120607819120607820AG37GENIChomozygous57632544
3120608362120608363CCTTT15GENIChomozygous58020878
3120608736120608737TA49GENIChomozygous58020880
3120608783120608784GA35GENIChomozygous58020882
3120608817120608818GGA37GENIChomozygous58020884
3120608919120608920AG33GENIChomozygous58020886
3120609516120609517TC54GENIChomozygous58020888
3120609799120609800TC34GENIChomozygous58020890
3120610193120610194TC27GENIChomozygous57632550
3120610563120610564CG29GENIChomozygous58020892
3120611030120611031CT48GENIChomozygous58020894
3120611412120611413AG29GENIChomozygous58020896
3120611620120611621CT49GENIChomozygous58020898
3120613084120613088GGGT----20GENIChomozygous58020900
3120613086120613088GT--22GENICpossibly homozygous57632552
3120613093120613094AG22GENICheterozygous58020902
3120613809120613810TG40GENIChomozygous58020904
3120613838120613839GA33GENIChomozygous58020906
3120614953120614954AG30GENIChomozygous57632556
3120615062120615063AG31GENIChomozygous58020908