chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144531945144531946TC3GENIChomozygous116101065
7144532862144532863GA33GENIChomozygous116101073
7144533287144533288AG27GENIChomozygous116101075
7144534451144534452AG18GENIChomozygous116101077
7144535288144535289GA19GENIChomozygous116101083
7144535327144535328GA23GENIChomozygous116101085
7144535402144535403GA27GENIChomozygous116101087
7144535789144535790GT16GENIChomozygous116101089
7144536464144536465GT15GENIChomozygous116101091
7144536488144536489GA19GENIChomozygous116101093
7144536557144536558AT18GENIChomozygous116101095
7144536682144536683AT22GENIChomozygous116101097
7144536700144536701TA24GENIChomozygous116101099
7144536868144536869AT20GENICpossibly homozygous116101101
7144537100144537101AG27GENIChomozygous115945474
7144538198144538199CT29GENIChomozygous116101103