chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84544671145446712AG66GENIChomozygous146465835
84544680645446807AT73GENIChomozygous138326142
84544730345447304G57GENIChomozygous146462163
84544766145447662CG45GENIChomozygous138326143
84544774445447745TC45GENIChomozygous138326144
84544912345449124AG48GENIChomozygous138326145
84544925845449259AG58GENIChomozygous138326146
84545013845450138TG42GENICpossibly homozygous146462164
84545028745450288CG61GENIChomozygous146465836
84545058245450583GA63GENIChomozygous146465837
84545067445450675CT60GENIChomozygous146465838
84545075645450757AT60GENIChomozygous138326148
84545280845452809TC56GENIChomozygous138326151
84545312445453128AGAC42GENIChomozygous146462165
84545491645454917AG60GENIChomozygous138326153
84545529645455297AG47GENIChomozygous146465839
84545536745455368TG50GENICpossibly homozygous146465840
84545636645456367AG34GENIChomozygous146465841
84545668445456685GA33GENIChomozygous138326154
84545668545456686TC31GENIChomozygous138326155
84545673345456734CT32GENIChomozygous146465842
84545817445458175GA61GENIChomozygous146465843
84545831645458317TC56GENIChomozygous146465844
84545676345456771CATTGTTT32GENIChomozygous138243721
84546032745460328CT43GENIChomozygous146465845
84546162845461629GA58GENIChomozygous146465846