chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37689027276890273GA53GENIChomozygous136755102
37689055276890553TG51GENIChomozygous136755103
37689195976891960CA40GENIChomozygous136755104
37689198576891986GA39GENIChomozygous136755105
37689207576892076TC47GENIChomozygous136755106
37689217676892177A34GENICpossibly homozygous136574165
37689257176892611ACTACTGGGAGGCCGCACATGCATGTGATATCACATGACA13GENIChomozygous136574166
37689338076893381GA55GENIChomozygous136755107
37689367976893680TC43GENIChomozygous136755108
37689470776894708GT41GENIChomozygous136755109
37689519776895198GA31GENIChomozygous136755110
37689540376895414ACAGAGGGTAA30GENIChomozygous136574167
37689559876895599AG25GENIChomozygous136755111
37689571876895726AAACAAAC20GENIChomozygous136574168
37689777976897780TA41GENIChomozygous136755112
37689836976898370G47GENIChomozygous136574169
37689837076898371TC47GENIChomozygous136755113