chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
84068779140687792G11GENICheterozygous403235221
84068779140687792GC11GENICheterozygous403235222
84068779340687794G11GENICheterozygous403235223
84068779340687794GC11GENICheterozygous403235224
84068779540687796G11GENICheterozygous403235225
84068779540687796GC11GENICheterozygous403235226
84068808740688088A30GENICheterozygous403235236
84068808740688088AC30GENICheterozygous403235237
84071313740713138G20GENICheterozygous403235239
84071313740713138GC20GENICheterozygous403235240
84072580140725802AT42GENICheterozygous154512045
84072720240727203AC22GENICheterozygous154512049
84072720240727203A22GENICheterozygous403235266
84071315840713159TC23GENICheterozygous138320708
84073895140738952GC24GENICpossibly homozygous138320709
84071315840713159T25GENICheterozygous403772185
84072371840723719CT46GENIChomozygous141018775
84072580140725802A42GENICheterozygous403621199
84080472340804724A20GENICheterozygous403772186
84080472340804724AT20GENICheterozygous403772187
84084526140845262TC21GENICheterozygous403830629
84084526140845262T21GENICheterozygous403830630
84085139340851394AG34GENICheterozygous154502881
84085139340851394A34GENICheterozygous403235327
84086719040867191T18GENICheterozygous403621219
84086719040867191TC18GENICheterozygous403621220
84083769040837690CA4GENICheterozygous141013735