chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13114826739114826742TTG---16GENICheterozygous49882076
13114826740114826742TG--15GENICheterozygous49882077
13114826741114826744GGG---14GENICheterozygous49882078
13114826743114826744G-14GENICheterozygous49882079
13114833017114833019GT--19GENICheterozygous50274497
13114838074114838075CT9GENIChomozygous49882085
13114838077114838078TG9GENICpossibly homozygous49882086
13114838088114838089GT9GENIChomozygous49882087
13114838092114838093GA10GENIChomozygous49882088
13114838116114838117TG13GENIChomozygous49882089
13114838127114838128GT12GENIChomozygous49882090
13114838131114838132GT11GENICpossibly homozygous49882091
13114838133114838134CT12GENIChomozygous49882092
13114838140114838141GT12GENIChomozygous49882093
13114838142114838143AT14GENIChomozygous49882094
13114838144114838145GT14GENIChomozygous49882095
13114838148114838149GT15GENIChomozygous49882096
13114838152114838153GT15GENIChomozygous49882097
13114839264114839265TG14GENICheterozygous49882098
13114846779114846780CA19GENICheterozygous49882105
13114862264114862265AG15GENICheterozygous49882112
13114870641114870642CCT18GENICheterozygous49882116