chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103515627235156273TG14GENIChomozygous781444279
103515631935156320TG36GENIChomozygous781444280
103515633135156332GA35GENIChomozygous781444281
103516860235168603CA49GENICpossibly homozygous781444282
103516877635168777CT38GENIChomozygous781444283
103517117535171176AG44GENIChomozygous781444284
103517264135172642GT48GENICpossibly homozygous781444285
103517488635174887CT76GENIChomozygous781444286
103517509335175094CA54GENIChomozygous781444287
103517509535175096GA53GENIChomozygous781444288
103517685035176851CT60GENIChomozygous781444289
103517701635177017GA61GENIChomozygous781444290
103517743335177434AG68GENIChomozygous781444291
103517970835179709CT71GENIChomozygous781444292
103518197235181973GC51GENIChomozygous781444293
103518212835182129CG73GENICpossibly homozygous781444294
103518291835182919TC58GENIChomozygous781444295
103518294735182948CT65GENIChomozygous781444296
103518326835183269GC69GENIChomozygous781444297
103518330135183302AG76GENIChomozygous781444298
103518464235184643AT25GENICheterozygous781444299
103518502335185024CG34GENIChomozygous781444300
103518521235185213GT17GENIChomozygous781444301
103518546435185465AC20GENIChomozygous781444302
103518559135185592GC36GENIChomozygous781444303
103518633235186333TC71GENIChomozygous781444304
103518643135186432AC75GENIChomozygous781444305
103518647935186480AG57GENIChomozygous781444306
103518825035188251GA71GENIChomozygous781444307
103518980435189805GA50GENIChomozygous781444308
103518985035189851AG45GENIChomozygous781444309
103519035035190351TA39GENICpossibly homozygous781444310
103519036735190368GA36GENICpossibly homozygous781444311
103519049035190491CT48GENIChomozygous781444312
103519087435190875GA59GENIChomozygous781444313
103519272935192730CT76GENICpossibly homozygous781444314
103519406835194069GC45GENIChomozygous781444315