chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
49590710795907108GA32GENIChomozygous137124169
49590763595907638AGA28GENIChomozygous136899832
49590800295908003GT19GENIChomozygous137124171
49590810595908106TC28GENIChomozygous137124172
49590898295908983TA23GENIChomozygous137124173
49591044995910450TC36GENIChomozygous137124175
49591076595910766AG36GENIChomozygous137124176
49591186295911863GA18GENIChomozygous137124178
49591269695912697AG20GENIChomozygous137124179
49591341595913416GT23GENIChomozygous137124180
49591384995913850G25GENIChomozygous136899834
49591436595914366TC39GENIChomozygous137124181
49591660795916608TC31GENICpossibly homozygous137124183
49591788095917881T22GENIChomozygous136899835
49591816895918169AG22GENIChomozygous144672151
49591504995915050TG17GENIChomozygous144672148
49591616095916161CT37GENIChomozygous144672149
49591722595917226CT31GENIChomozygous144672150
49591884895918849TC28GENIChomozygous144672152