chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
118386873683868737GC27GENIChomozygous51077998
118386877983868780GA26GENIChomozygous51027096
118386882883868829AG28GENIChomozygous51027098
118386883883868839TC28GENIChomozygous51027099
118386884083868841CG28GENIChomozygous51027100
118386885383868862AACAAGAAC---------30GENIChomozygous51027101
118386911183869112T-26GENIChomozygous51027104
118386914583869146TA17GENIChomozygous51078000
118386915583869156GT22GENIChomozygous51027105
118386918283869183TC18GENIChomozygous51027106
118386918683869187GA17GENIChomozygous51027107
118386919983869200CA17GENIChomozygous51027108
118386926683869267CA17GENIChomozygous51027109
118386927083869271GA15GENIChomozygous51027110
118386930483869305TTCACA8GENICheterozygous51229514
118386930483869305TTCACACACACA8GENICheterozygous51229515
118386932783869328TC24GENICheterozygous51027111
118386936583869366TA19GENIChomozygous51027112
118386937783869378TA22GENIChomozygous51027113
118386964583869646GT26GENIChomozygous51078002
118386998583869986TA28GENIChomozygous51078004
118387052683870527AG26GENIChomozygous51027118
118387057283870573GA26GENIChomozygous51078006
118387066683870667CT35GENIChomozygous51027119
118387070183870702TC24GENIChomozygous51027120
118387097483870975TG33GENIChomozygous51078008
118387169283871693TC34GENIChomozygous51027124
118387204583872046AG21GENIChomozygous51027128
118387256883872569AG33GENIChomozygous51027139
118387298883872989GA18GENIChomozygous51078010