chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109104157091041576TTTGTT56GENIChomozygous131902759
109104205791042058GT37GENIChomozygous116821622
109104281591042816CT61GENIChomozygous116821624
109104396791043968CT54GENIChomozygous116821626
109104457291044593GGTCCTGAGCTAGGGTAAGAC35GENIChomozygous131902760
109104486291044863TC44GENIChomozygous116821628
109104494591044945A30GENICpossibly homozygous131902761
109104512491045125CA39GENIChomozygous116821630
109104597791045978AG50GENIChomozygous116821638
109104609991046100TG55GENICpossibly homozygous116821640
109104260491042605TC46GENIChomozygous116905267
109104578291045783TA53GENIChomozygous116905271
109104302191043022GA40GENIChomozygous117088085
109104427391044274CT53GENIChomozygous117088087