chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2228504627228504628CA9GENIChomozygous815850109
2228504628228504629CA9GENIChomozygous815850110
2228504636228504637A-10GENIChomozygous815850111
2228504640228504641TC11GENIChomozygous815850112
2228504686228504687TC14GENIChomozygous815850113
2228504691228504692T-13GENIChomozygous815850114
2228505272228505273TC21GENIChomozygous815850115
2228505292228505293AAT17GENIChomozygous815850116
2228505606228505607CT15GENIChomozygous815850117
2228505670228505671CT17GENIChomozygous815850118
2228506041228506042TC15GENIChomozygous815850119
2228506283228506299TTTGTTTGTTTGTTTG----------------7GENIChomozygous815850120
2228506325228506326TC13GENIChomozygous815850121
2228506491228506492CT22GENIChomozygous815850122
2228506503228506504CT17GENIChomozygous815850123
2228506548228506549CT18GENIChomozygous815850124
2228506621228506622AG20GENIChomozygous815850125
2228506779228506780GA19GENIChomozygous815850126
2228507182228507183AG17GENIChomozygous815850127
2228507496228507497CG11GENIChomozygous815850128
2228508507228508508TA11GENIChomozygous815850129
2228508825228508826GA10GENIChomozygous815850130
2228508827228508828GA9GENIChomozygous815850131
2228508897228508904GGGTTTA-------7GENIChomozygous815850132
2228509044228509045T-5GENIChomozygous815850133
2228509046228509049TGC---5GENIChomozygous815850134
2228509053228509061GCGTGTGC--------6GENIChomozygous815850135
2228509066228509067CT6GENIChomozygous815850136
2228509072228509073CT6GENIChomozygous815850137
2228509078228509079CT7GENIChomozygous815850138
2228509084228509085CT6GENIChomozygous815850139
2228509255228509256AC12GENIChomozygous815850140
2228509321228509322TA16GENIChomozygous815850141
2228509339228509340TC17GENIChomozygous815850142
2228509520228509521CT11GENIChomozygous815850143
2228509594228509595GA16GENIChomozygous815850144
2228509664228509665CT12GENIChomozygous815850145