chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113037401230374013AT14GENIChomozygous115959551
113037429630374297CT23GENIChomozygous115808379
113037533030375331TC29GENIChomozygous115808381
113038458430384585AC28GENIChomozygous115808383
113038493030384931GA24GENIChomozygous115808385
113038573530385736TA19GENIChomozygous115808387
113038600330386004AG24GENIChomozygous115808389
113038712430387125CT28GENIChomozygous115808391
113039043530390436AT29GENIChomozygous115808393
113039099230390993GT39GENIChomozygous115808395
113039357630393577GC25GENIChomozygous115808397
113039486530394866GA29GENIChomozygous115808399
113039727430397275CT29GENICpossibly homozygous115808401
113040284630402847CT19GENIChomozygous115808403
113041271130412712AG21GENIChomozygous115808405
113041306930413070AG40GENIChomozygous115808407
113041320530413206AC21GENIChomozygous115808409
113041478730414788CT28GENIChomozygous115808411
113041478930414790GA30GENIChomozygous115808413
113041528730415288TG26GENIChomozygous115808415
113041557630415577TA25GENIChomozygous115808419
113042153930421540TA29GENIChomozygous115959571
113042346330423464AG26GENIChomozygous115808421
113042395730423958GT21GENIChomozygous115808423
113042545930425460AG6GENIChomozygous116035188
113042645730426458TA27GENIChomozygous115808425