chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2226855227226855228AC19GENIChomozygous60083292
2226855237226855238CCA22GENIChomozygous60083293
2226855276226855277CT26GENIChomozygous60083294
2226855851226855852AG32GENIChomozygous59421517
2226855945226855946TC25GENIChomozygous60083295
2226856200226856201CT27GENIChomozygous60083296
2226856464226856465GC18GENIChomozygous60302999
2226857181226857183TA--28GENIChomozygous60083297
2226857459226857460GA26GENIChomozygous60303000
2226857815226857816TC22GENIChomozygous60083298
2226858271226858272AG23GENIChomozygous60083300
2226858667226858668T-19GENIChomozygous60303001
2226858770226858771GA24GENIChomozygous60303002
2226858968226858976TGCGTGCA--------13GENIChomozygous60303003
2226860009226860010GA19GENIChomozygous60303005
2226860263226860264A-27GENIChomozygous60303006
2226860314226860315CT23GENIChomozygous60303007
2226860315226860316AG23GENIChomozygous60303008
2226860365226860366TG30GENIChomozygous60303009
2226860875226860876TC25GENIChomozygous60083303
2226861138226861139CT26GENIChomozygous60303010
2226856962226856963TG14GENIChomozygous60519823
2226861673226861677AGGT----26GENICpossibly homozygous60519824
2226861679226861680AG26GENICpossibly homozygous60519825
2226861683226861684AAGG26GENICpossibly homozygous60519826
2226862064226862065CCCCTCT9GENIChomozygous60519827
2226862175226862176TTCA12GENIChomozygous60303011
2226863523226863524CT22GENIChomozygous60303012
2226863715226863716TC20GENIChomozygous60083310
2226863967226863968AG17GENIChomozygous60303013
2226863982226863983CT17GENIChomozygous60303014
2226864886226864887T-15GENIChomozygous60083312
2226865440226865441G-25GENIChomozygous60303015
2226867488226867489CT19GENIChomozygous60303016
2226868248226868249GGT14GENIChomozygous59421521