chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56355952063559521CCT15GENICpossibly homozygous55880099
56356113863561139CT33GENIChomozygous55880103
56356442463564425TC39GENIChomozygous55424614
56356537563565376TC26GENIChomozygous55424615
56356678963566790GA30GENIChomozygous55424618
56357061063570611TTAGTCGACCCTCTTGG33GENIChomozygous55424627
56357422463574225GT27GENIChomozygous55880105
56357453563574536CT26GENICpossibly homozygous55424628
56357514963575150CT41GENIChomozygous55424631
56357520463575205GA32GENIChomozygous55880107
56357532663575327GGA28GENIChomozygous55424633
56357626663576267AG19GENIChomozygous55424641
56357648263576483CCA15GENICpossibly homozygous55880111
56357708563577086GA34GENIChomozygous55880113
56358662563586626AAT34GENIChomozygous55424673
56358319763583198TTA24GENIChomozygous55880115
56358599863585999CT39GENIChomozygous55880117
56358604963586050GA32GENIChomozygous55880119
56357532863575329GA30GENIChomozygous56347956
56358716863587169AT34GENIChomozygous55424675
56358794163587942T-20GENIChomozygous55880121