chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13114826741114826747GGGTTC------14GENICheterozygous50537003
13114826743114826744G-14GENICpossibly homozygous49882079
13114832856114832857AAT12GENICheterozygous49882082
13114838019114838020AC9GENICpossibly homozygous50537007
13114838074114838075CT18GENIChomozygous49882085
13114838077114838078TG18GENIChomozygous49882086
13114838088114838089GT22GENIChomozygous49882087
13114838092114838093GA23GENIChomozygous49882088
13114838116114838117TG15GENIChomozygous49882089
13114838127114838128GT18GENIChomozygous49882090
13114838131114838132GT19GENIChomozygous49882091
13114838133114838134CT20GENIChomozygous49882092
13114838140114838141GT21GENIChomozygous49882093
13114838142114838143AT22GENIChomozygous49882094
13114838144114838145GT23GENIChomozygous49882095
13114838148114838149GT24GENIChomozygous49882096
13114838152114838153GT25GENIChomozygous49882097
13114869953114869955CA--8GENICheterozygous50537009