chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2185046086185046087CT18GENIChomozygous59285702
2185049257185049258CT7GENIChomozygous60066220
2185051101185051102TA4GENIChomozygous59285708
2185051900185051901C-20GENIChomozygous59285711
2185052450185052452TA--2GENICheterozygous59285712
2185052470185052471A-4GENIChomozygous59285713
2185053004185053005CT8GENIChomozygous59285714
2185053365185053366TC16GENICpossibly homozygous60066224
2185054102185054103CT19GENIChomozygous59285715
2185054286185054287AC24GENIChomozygous60066226
2185056575185056576CT17GENIChomozygous60066228
2185056868185056869TC25GENIChomozygous59285718
2185057480185057481CT10GENIChomozygous59285720
2185057493185057494GT10GENICpossibly homozygous60066230
2185059050185059051GA15GENICheterozygous59285722
2185059235185059236TC11GENICpossibly homozygous59285723
2185062800185062801AC16GENIChomozygous60066234
2185063532185063533TC8GENIChomozygous59285731
2185064430185064431GGTTA6GENIChomozygous59285732
2185065813185065814T-1GENIChomozygous59907427
2185066141185066142AC2GENIChomozygous60066236
2185066763185066764AG4GENICheterozygous59285734
2185067253185067254AG4GENIChomozygous59285735
2185068666185068667CT5GENIChomozygous59285737
2185069408185069409TC13GENIChomozygous60066238
2185072314185072315AAGTGTGTGT6GENICheterozygous60560691
2185073197185073198CT15GENICpossibly homozygous61464185
2185074813185074814G-3GENIChomozygous59907432
2185073506185073507TTATAC4GENIChomozygous61403380
2185079427185079428A-9GENIChomozygous59907436
2185083077185083078AG13GENICpossibly homozygous59285758
2185083930185083931AT7GENICheterozygous59285759
2185084889185084890T-5GENIChomozygous60066246
2185086048185086049TG12GENIChomozygous59285762
2185086114185086115T-3GENIChomozygous59285763
2185086556185086557GT7GENIChomozygous59285764
2185088524185088525TA21GENIChomozygous60066248
2185091124185091125AG20GENICpossibly homozygous59285766
2185100221185100222CG6GENICheterozygous59285777