chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
158613620086136201TC14GENIChomozygous112946395
158613840586138406GA22GENIChomozygous112570549
158613685086136851TC30GENIChomozygous112570541
158613697486136975TC23GENIChomozygous112570543
158613737786137378AT28GENIChomozygous112570545
158613816886138169TC46GENIChomozygous112570547
158613883286138833TC8GENIChomozygous112570551
158613892386138924AC12GENIChomozygous112570552
158613905186139052AG38GENIChomozygous112570554
158613909886139099AT34GENIChomozygous112570556
158613975586139756GA26GENIChomozygous112570558
158613977986139780AG21GENIChomozygous112570561
158613996486139965GT18GENICpossibly homozygous112570563
158614003486140035CT17GENICpossibly homozygous112570565
158614033986140340CT22GENIChomozygous112570567
158614045386140454GC25GENIChomozygous112570569
158614154686141547GC25GENIChomozygous112570571
158614172486141725GA16GENIChomozygous112570573