chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124988935349889354GGGTGTGTGTGTGTGTGTGT5GENIChomozygous741287797
124989068949890690AAC6GENICheterozygous741287799
124989172049891730ACACACACAC----------2GENIChomozygous741287801
124989195249891953TC18GENIChomozygous616722442
124989251549892516AG9GENIChomozygous616722443
124989256449892565CCG14GENIChomozygous741287803
124989299449892995AG22GENIChomozygous616722444
124989300649893007CT19GENIChomozygous616722445
124989532949895330GA15GENIChomozygous616722446
124989590749895908AC15GENIChomozygous616722447
124989666049896661CG6GENIChomozygous616722448
124989682749896828GA7GENIChomozygous616722449
124989710549897106GC12GENIChomozygous616722450
124989727349897274CT9GENIChomozygous616722451
124989737749897378CT16GENIChomozygous616722452
124989803049898031CT11GENIChomozygous616722453
124989904349899044TC15GENIChomozygous616722454
124989964349899645TG--21GENIChomozygous741287804
124989994049899941AAATAGGTAAGGGGTAGCTAGAAATGGGGACACTGAGACTGGTCAGGTCACACAGGTT27GENIChomozygous741287805
124990007949900080CT11GENIChomozygous616722455
124990069149900692GA10GENIChomozygous616722456
124990257749902578GA5GENIChomozygous616722457
124990260349902607GGAG----3GENIChomozygous741287806
124990313049903131CA13GENICpossibly homozygous616722458
124990487949904883AAAA----6GENIChomozygous741287808
124990488249904883AACC6GENIChomozygous741287810
124990714049907141AT6GENIChomozygous616722459