chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62887872128878722AAACAC5GENICheterozygous54310164
62887872228878724AC--5GENICheterozygous54310167
62888909628889097G-61GENICheterozygous54310170
62890420728904208CA17GENIChomozygous54310174
62890420928904210AT16GENIChomozygous54310177
62890421528904216GA16GENIChomozygous54310180
62890422828904229TA17GENIChomozygous54310184
62890423128904232TC18GENIChomozygous54310187
62890423928904240T-17GENIChomozygous54310190
62890425228904253CG14GENIChomozygous54310193
62890426428904265TC17GENIChomozygous54310196
62890427128904272CA15GENIChomozygous54310199
62890427228904273CT15GENIChomozygous54310203
62890430828904309TA24GENIChomozygous54310205
62890432328904324AT22GENIChomozygous54310208
62890435228904353TA24GENIChomozygous54829657
62890437028904371AAT25GENIChomozygous54310211
62890437728904378TA30GENIChomozygous54310213
62890561028905611AG75GENICheterozygous54310219
62890565328905656AGC---40GENICheterozygous54310222
62890587428905877GGG---4GENICheterozygous54829672
62890588228905885GCG---5GENICheterozygous54829674
62891110528911106T-12GENICheterozygous54310234
62891117928911180A-2GENIChomozygous54310237
62891119828911199TTC2GENIChomozygous54310240
62890770028907701TG35GENICheterozygous55310219
62892690928926910TG28GENIChomozygous54310243
62892709328927094CCG22GENIChomozygous54310249
62892709728927098C-20GENIChomozygous54310252
62892710428927105GC23GENICpossibly homozygous54310255