chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134954679249546793TC22GENICpossibly homozygous114616983
134954821449548215TC28GENIChomozygous114616985
134954824449548245TC33GENIChomozygous114616987
134954858749548588GA18GENIChomozygous114616989
134954913949549140TC20GENIChomozygous114616991
134954960249549603AC32GENIChomozygous114670566
134954970349549704GT32GENIChomozygous114616993
134955040649550407TC9GENIChomozygous114823905
134955069249550693CT31GENIChomozygous114616996
134955224749552248AG19GENIChomozygous114616998
134955230349552304GA22GENIChomozygous114617000
134955270449552705GC31GENIChomozygous114617002
134955288449552885GA27GENIChomozygous114617004
134955406949554070GA21GENIChomozygous114617006
134955409549554096TC25GENIChomozygous114617008
134955419249554193AG26GENIChomozygous114617009
134955439549554396GA22GENIChomozygous114617011
134955526849555269AC39GENICpossibly homozygous114617013
134955594549555946TC28GENIChomozygous114617015
134955626849556269GA30GENIChomozygous114617021
134955709249557093CT22GENIChomozygous114617023
134955752349557524TA22GENIChomozygous114617025
134955771649557717TG24GENIChomozygous114617027
134955776149557762GA28GENIChomozygous114617029
134955776949557770GA26GENIChomozygous114617031
134955788449557885AG26GENIChomozygous114617033
134955789549557896TG25GENIChomozygous114617035
134955794649557947GA26GENIChomozygous114617037
134955802849558029AG23GENIChomozygous114617039
134955981849559819GA21GENIChomozygous114617041
134955992249559923AG24GENIChomozygous114617043
134955994249559943AC26GENIChomozygous114617045
134956033349560334CT9GENIChomozygous114617047
134956034849560349TA7GENIChomozygous114617049
134956035249560353CT7GENIChomozygous114617051
134956042949560430TC3GENIChomozygous114670570
134956043249560433CG3GENIChomozygous114670572
134956055349560554TC18GENIChomozygous114670574
134956058649560587AC16GENIChomozygous114617052
134956061849560619CT19GENIChomozygous114617054