chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103635726836357269AAGAGAGAGAGAGAGAGG10GENIChomozygous52316260
103635728936357290GA10GENIChomozygous51413770
103635738636357387AG42GENIChomozygous51413772
103635757136357572CT39GENIChomozygous51413774
103635778636357787TC40GENIChomozygous51413776
103635779536357796TC47GENIChomozygous51413778
103635860836358611AAG---50GENIChomozygous51413780
103635885236358853AG22GENIChomozygous51413782
103635901036359018CTGGGCTA--------39GENIChomozygous51413784
103635934136359342GA43GENIChomozygous51413786
103636008236360083AATG28GENIChomozygous51413788
103636096336360964AG50GENIChomozygous51413790
103636117136361172GA47GENIChomozygous51413792
103636342436363425CG40GENIChomozygous51413794
103636411136364112AT33GENIChomozygous51413796
103636440836364409TC41GENIChomozygous51413798
103636481836364820AG--47GENIChomozygous51413800
103636660936366610GA29GENIChomozygous51413802
103636705436367055AAG38GENIChomozygous51413804
103636709436367095GGTT24GENICpossibly homozygous51413806
103636709436367095GGTTT24GENICheterozygous51634402
103636723236367233CT18GENIChomozygous51413810
103636727936367280T-28GENIChomozygous51413812
103636731936367320GGGGT24GENIChomozygous51413815
103636733236367333TTG21GENIChomozygous51413817
103636733636367337TG21GENIChomozygous52316261
103636738436367385AG29GENIChomozygous51413821
103636745536367456CT40GENIChomozygous51413823
103636750636367507CT49GENIChomozygous51413825
103636836736368368GA19GENIChomozygous51413827
103637063936370640A-20GENIChomozygous51413829