chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46308920363089204TC25GENIChomozygous112673998
46309003063090031AG53GENICpossibly homozygous112674000
46309041263090413TC15GENIChomozygous112674002
46309117563091176AC48GENIChomozygous112674004
46309129263091293AG48GENIChomozygous112674006
46309140263091403CT12GENIChomozygous112674008
46309143563091436TC9GENIChomozygous112674010
46309166663091667CA29GENIChomozygous112674012
46309176463091765AG38GENIChomozygous112674014
46309185363091854AT48GENIChomozygous112674016
46309280563092806TC43GENIChomozygous112674018
46309285063092851TG35GENIChomozygous112674020
46309343463093435TC21GENIChomozygous112674022
46309589663095897AC21GENIChomozygous112674036
46309630663096307AG27GENIChomozygous112674038
46309636563096366AC35GENIChomozygous112674040
46309638563096386CT48GENIChomozygous112674042
46309657163096572CG28GENIChomozygous112674044
46309658863096589GT24GENIChomozygous112674046
46309663663096637CT12GENIChomozygous112674048
46309717263097173AT25GENIChomozygous112674050
46309777663097777TG37GENIChomozygous112674052
46309819063098191TG41GENIChomozygous112674054
46309820563098206TC51GENIChomozygous112674056
46309873963098740AG33GENIChomozygous112674058
46309999363099994TG20GENIChomozygous112674060
46310087363100874GA38GENIChomozygous112674064
46310135363101354GA52GENIChomozygous112674066
46310243563102436TC18GENIChomozygous112674068
46310257963102580CT25GENIChomozygous112674070
46310369263103693AG14GENIChomozygous112674072
46310469663104697AC52GENIChomozygous112674074
46310567963105680CT11GENIChomozygous112674076