chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
19017837090178371GA27GENICpossibly homozygous622692210
19017892590178926AG12GENIChomozygous622692211
19018145790181458AC19GENICpossibly homozygous622692212
19018190490181905AAT1GENIChomozygous740026823
19018405790184058G-3GENIChomozygous740026826
19018419990184200TC6GENIChomozygous622692213
19018445890184459TA11GENIChomozygous622692214
19018452590184526AG23GENICpossibly homozygous622692215
19018477490184775GC19GENICpossibly homozygous622692216
19018758190187585CTCT----3GENICheterozygous740026827
19018885390188860GGCCTGT-------1GENIChomozygous740026829
19018887890188879TC2GENIChomozygous622692217
19019130890191309AG33GENICpossibly homozygous622692218
19019186790191868A-1GENIChomozygous740026830
19019325590193256AT8GENICheterozygous622692219
19019346390193464GA14GENICpossibly homozygous622692220
19019620390196204GGCACTGGT3GENICheterozygous740026832
19019620590196206AAAAC3GENICheterozygous740026833