chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139851603498516035GA15GENIChomozygous49866231
139851834298518343TC16GENIChomozygous49866242
139851859898518599AAT8GENIChomozygous49866243
139851861998518620GA15GENIChomozygous49866244
139851906398519064CCA19GENIChomozygous49866245
139851979498519795GC14GENIChomozygous49866246
139852127698521278TT--8GENIChomozygous49866248
139852141898521419GA14GENICpossibly homozygous49866249
139852218998522190CCA8GENIChomozygous49866252
139852268298522683TC13GENICheterozygous49866254
139852363298523633TC15GENICpossibly homozygous49866277
139852390798523908CT12GENIChomozygous49866278
139852402098524021AG24GENIChomozygous49866279
139852557798525578CT27GENIChomozygous49866280
139852563598525636TC18GENIChomozygous49866281
139852635298526353CT24GENICpossibly homozygous49866282
139852688498526885CT28GENIChomozygous49866283
139852756398527564GA7GENIChomozygous49866284
139852786698527867CT11GENIChomozygous49866285
139852829298528293CT7GENIChomozygous49866286
139852865498528655CT6GENIChomozygous49866288
139852932898529329AC13GENICpossibly homozygous49866291
139852938498529385CT10GENIChomozygous49866292
139852949598529496TC14GENIChomozygous49866293
139852995098529951C-1GENIChomozygous50553855
139853014398530144CA19GENICheterozygous49866296
139853070198530702TC4GENIChomozygous49866297
139853070398530704T-4GENIChomozygous49866298
139853092498530925CT13GENICpossibly homozygous49866299
139853095698530957TTA9GENIChomozygous49866300
139853104998531050TA9GENIChomozygous49866301
139853110298531103GA17GENIChomozygous49866302
139853111098531111TC12GENIChomozygous49866303
139853121698531217CG13GENIChomozygous49866304
139853202698532027TC14GENIChomozygous49866305
139853229398532294TC6GENIChomozygous49866306
139853335798533358TA20GENICpossibly homozygous49866307
139853340098533401TC18GENICpossibly homozygous49866308
139853397498533975GA11GENICheterozygous49866310
139853548098535481GT6GENIChomozygous49866311
139853807398538074C-7GENIChomozygous49866312