chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106753826167538262AG18GENICheterozygous51682328
106754253867542539GGC4GENIChomozygous51480666
106754253967542540AT4GENIChomozygous52320516
106754254267542543AT4GENIChomozygous51480667
106757731667577317GA20GENICpossibly homozygous52996445
106758513867585139GA12GENICheterozygous51910419
106759356867593686TTGAAAAATATTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGATCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC----------------------------------------------------------------------------------------------------------------------12GENICheterozygous52320520
106760709367607094GA22GENICpossibly homozygous51480672
106762343267623433GA17GENICheterozygous52320524
106767694767676948CT36GENICpossibly homozygous51480682
106767913067679131TC14GENICheterozygous51910780
106771108267711083AAAC4GENICheterozygous51682671
106771111067711111TC13GENICheterozygous51911014
106772858267728583AG8GENICheterozygous51911156
106772979367729794AG16GENICheterozygous51480688
106772979467729795AG16GENICheterozygous51480689
106773145467731455TTG6GENIChomozygous51480690
106773146067731461GGT8GENIChomozygous51480691
106774496267744966TCTG----7GENICheterozygous52996447
106778308267783083AAGTGT1GENIChomozygous52440996
106780388867803889AG12GENIChomozygous51480702
106780745067807451AAG23GENIChomozygous51480703