chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134375586243755874ACCCACCCACCT15GENIChomozygous144924871
134375699143756991CT46GENICpossibly homozygous144924872
134375737343757374AC50GENIChomozygous144930139
134375740943757409G50GENIChomozygous144924873
134375773043757731GT42GENIChomozygous144930140
134375806343758064GA54GENIChomozygous144930141
134375867543758676CT59GENIChomozygous144930142
134375928043759281AG50GENIChomozygous144930143
134375968043759681CT35GENIChomozygous144930144
134375986043759861TC42GENIChomozygous144930145
134376050743760508CA53GENIChomozygous144930146
134376066343760664TC46GENIChomozygous144930147
134376465743764658GA46GENIChomozygous144930148
134376590443765905TC57GENIChomozygous144930149
134376681443766815CT47GENIChomozygous144930150
134376865843768659TC44GENIChomozygous144930151
134376898343768984CT47GENIChomozygous144930152
134376952243769523GA56GENIChomozygous144930153
134376961243769613TC53GENIChomozygous144930154
134377029843770299C37GENIChomozygous144924874
134376926743769268AG55GENIChomozygous142367267
134376390143763902CT20GENICheterozygous154798049
134377029843770299CT37GENICheterozygous154798050
134376390143763902C20GENICheterozygous403337778