chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144939803144939804AC3GENICheterozygous126621024
7144942587144942588CT15GENIChomozygous115946160
7144944071144944072CT20GENIChomozygous115946162
7144944613144944614CT6GENIChomozygous115946163
7144944617144944618CT8GENIChomozygous115946165
7144944663144944664AG8GENIChomozygous115946167
7144944913144944914GA15GENIChomozygous115946169
7144945531144945532GT8GENIChomozygous115946171
7144945850144945851CT13GENIChomozygous115946175
7144945588144945589CG18GENIChomozygous126541799
7144945734144945735GA11GENICheterozygous126588224
7144945769144945770AG17GENIChomozygous115946173
7144953382144953383CT18GENIChomozygous115946189
7144953638144953639CA8GENIChomozygous115946191
7144954095144954096GA19GENIChomozygous115946193
7144955952144955953CT11GENIChomozygous115946197
7144958429144958430CT12GENIChomozygous115946199
7144961041144961042AG19GENIChomozygous115946205
7144964059144964060AG22GENIChomozygous115946207
7144964293144964294TC19GENIChomozygous115946209
7144964446144964447GT3GENICheterozygous116101387
7144964894144964895CT18GENIChomozygous115946211
7144965235144965236CG16GENIChomozygous126541800
7144965261144965262CG5GENIChomozygous126541801
7144965288144965289AG4GENIChomozygous126541804