chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17897652078976521AC33GENIChomozygous986939286
17897652978976530CT34GENIChomozygous986939287
17897686378976864GA28GENIChomozygous986939288
17897704278977043GC39GENIChomozygous986939289
17897712078977121CT46GENIChomozygous986939290
17897762678977627TC29GENIChomozygous986939291
17897819578978196TC70GENIChomozygous986939292
17897889978978900CT23GENIChomozygous986939293
17897920778979208TA31GENIChomozygous986939294
17897927378979274CT45GENIChomozygous986939295
17897934178979342GA34GENIChomozygous986939296
17897938978979390CT28GENIChomozygous986939297
17897966278979663CT36GENIChomozygous986939298
17898330978983310AT40GENIChomozygous986939299
17898381078983811TC31GENIChomozygous986939300
17898403978984040TG47GENIChomozygous986939301
17898535578985356TC42GENIChomozygous986939302
17898739078987391GA32GENIChomozygous986939303
17898771378987714TC24GENIChomozygous986939304
17898773078987731AC21GENIChomozygous986939305
17898867678988677CT22GENIChomozygous986939306
17898947678989477GA53GENIChomozygous986939307
17898995778989958TC20GENIChomozygous986939308
17899010278990103AG24GENIChomozygous986939309
17899063378990634GA32GENIChomozygous986939310
17899081078990811CT28GENIChomozygous986939311
17899097878990979TC28GENIChomozygous986939312
17899258778992588AG29GENIChomozygous986939313
17899274978992750TC31GENIChomozygous986939314
17899300878993009TC22GENIChomozygous986939315
17899385278993853CT23GENIChomozygous986939316
17899446978994470CT30GENIChomozygous986939317
17899461278994613GA15GENIChomozygous986939318
17899562578995626CT29GENIChomozygous986939319
17899567078995671AT31GENIChomozygous986939320
17899595378995954CT44GENIChomozygous986939321
17899644878996449TG19GENIChomozygous986939322