chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13114826741114826747GGGTTC------20GENICheterozygous50537003
13114826743114826744G-20GENICpossibly homozygous49882079
13114831570114831571T-15GENICheterozygous50537005
13114834538114834542GTGT----5GENICheterozygous50587406
13114838019114838020AC13GENIChomozygous50537007
13114838074114838075CT20GENIChomozygous49882085
13114838077114838078TG21GENIChomozygous49882086
13114838088114838089GT28GENIChomozygous49882087
13114838092114838093GA27GENIChomozygous49882088
13114838116114838117TG32GENIChomozygous49882089
13114838127114838128GT27GENIChomozygous49882090
13114838131114838132GT27GENIChomozygous49882091
13114838133114838134CT27GENIChomozygous49882092
13114838140114838141GT27GENIChomozygous49882093
13114838142114838143AT29GENIChomozygous49882094
13114838144114838145GT30GENIChomozygous49882095
13114838148114838149GT31GENIChomozygous49882096
13114838152114838153GT31GENIChomozygous49882097
13114846834114846835GGT4GENICheterozygous50566903
13114869953114869955CA--14GENICheterozygous50537009