chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4220863861220863862GT28GENIChomozygous575138527
4220865688220865689GGTGTGTGTGTGTA29GENICpossibly homozygous714180694
4220865950220865951TC30GENIChomozygous575138528
4220866163220866164AAACAGTCTC33GENIChomozygous714180695
4220866308220866309CT33GENIChomozygous575138529
4220867182220867183CT52GENIChomozygous575138530
4220867457220867458GT42GENIChomozygous575138531
4220867545220867546AT37GENIChomozygous575138532
4220870021220870022TC35GENIChomozygous575138533
4220870972220870973AATTTT16GENIChomozygous714180696
4220872787220872788TA31GENIChomozygous575138534
4220873146220873147TC32GENIChomozygous575138535
4220873722220873728ACACAC------10GENICpossibly homozygous714180697
4220873953220873954TC46GENIChomozygous575138536
4220875508220875509CCTTT18GENICpossibly homozygous714180699
4220875601220875602T-13GENICheterozygous714180700
4220875728220875729TTA34GENIChomozygous714180701
4220877048220877049GGGTGTGTGT21GENIChomozygous714180702
4220877136220877137GGTCTCTC37GENICpossibly homozygous714180703
4220877136220877137GGTCTCTCTC37GENICheterozygous714180704
4220877136220877137GGTCTC37GENICheterozygous714180705
4220877271220877272CG66GENICpossibly homozygous575138537
4220877449220877450CCTGTG23GENIChomozygous714180707
4220877514220877516TC--30GENIChomozygous714180708
4220877584220877586TC--43GENICpossibly homozygous714180709
4220877696220877697GT9GENIChomozygous575138538
4220877700220877701GT6GENIChomozygous575138539
4220879291220879292GA21GENIChomozygous575138540
4220880183220880184CT23GENIChomozygous575138541
4220880485220880486GA30GENIChomozygous575138542
4220880567220880568AG36GENIChomozygous575138543
4220880591220880592AC35GENIChomozygous575138544