chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4187412243187412244GA22GENIChomozygous59658996
4187412259187412260GA19GENIChomozygous59658997
4187412745187412746GA28GENICpossibly homozygous59658998
4187413187187413188CT31GENIChomozygous58870174
4187413247187413248AG33GENIChomozygous59658999
4187414000187414003GGT---23GENIChomozygous59659000
4187414901187414902TG31GENIChomozygous59659001
4187415085187415086TG27GENICpossibly homozygous59659002
4187415125187415126GA30GENICpossibly homozygous59659003
4187415607187415608GA40GENICpossibly homozygous59659004
4187415800187415801TA40GENIChomozygous59659005
4187416366187416367TC17GENIChomozygous59659006
4187416721187416722CT30GENIChomozygous59659007
4187417487187417488AG37GENIChomozygous59659008
4187417506187417507GGAA35GENIChomozygous59659009
4187417508187417509T-35GENIChomozygous59659010
4187417511187417512C-34GENIChomozygous59659011
4187417512187417513CA33GENIChomozygous59659012
4187417724187417732CCCACACA--------25GENIChomozygous59659013
4187418544187418545TA30GENIChomozygous59659014
4187418768187418769CT29GENIChomozygous59659015
4187421921187421922GA33GENIChomozygous59659016
4187422783187422784GA20GENIChomozygous59659017
4187423005187423006TC32GENIChomozygous57564585
4187423421187423422CT18GENIChomozygous59659018
4187424994187424995GC31GENIChomozygous57564592
4187425047187425048CT33GENIChomozygous57564594
4187425338187425339TC24GENIChomozygous59659019
4187424658187424659GA24GENIChomozygous58678743