chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4153351552153351553AG27GENIChomozygous112889515
4153351623153351624AG13GENIChomozygous112889516
4153353221153353222CT17GENIChomozygous112889518
4153353450153353451GA5GENIChomozygous112889519
4153353652153353653GA13GENIChomozygous112889520
4153353674153353675GA12GENIChomozygous112889521
4153354719153354720AG22GENIChomozygous112889522
4153355113153355114GA17GENIChomozygous112889524
4153355185153355186CT12GENIChomozygous112889525
4153355354153355355CA19GENIChomozygous112889526
4153356038153356039CT15GENIChomozygous112889527
4153356344153356345CT21GENIChomozygous112889528
4153356813153356814AG17GENIChomozygous112889530
4153357001153357002AG13GENIChomozygous112889531
4153357449153357450GA16GENIChomozygous112889532
4153358700153358701TC14GENIChomozygous112889535
4153360104153360105CT27GENIChomozygous112889536
4153360337153360338GA17GENIChomozygous112889537
4153360433153360434GA14GENIChomozygous112889538
4153360595153360596CT19GENIChomozygous112889539
4153361114153361115AT19GENIChomozygous112889540
4153361322153361323AC14GENIChomozygous112889541
4153361369153361370TA21GENIChomozygous112889542
4153363002153363003AG2GENIChomozygous112889544
4153363698153363699GA28GENIChomozygous112889545
4153364151153364152CG27GENIChomozygous112889546
4153366707153366708TC10GENIChomozygous112889548
4153367806153367807CA8GENIChomozygous119282183
4153368288153368289TA16GENIChomozygous112889553
4153369136153369137GC22GENIChomozygous112889555
4153370520153370521AG11GENIChomozygous112889556
4153371568153371569AC8GENIChomozygous112889558