chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103635723236357233GGGAGAGA2GENIChomozygous52435676
103635903436359035T-19GENIChomozygous52040293
103636440836364409TC51GENIChomozygous51413798
103636660936366610GA66GENIChomozygous51413802
103636709436367095GGTT12GENICheterozygous51413806
103636709436367095GGTTT12GENICpossibly homozygous51634402
103636721836367219GA11GENIChomozygous52040295
103636722536367226TTTTTC7GENIChomozygous51413808
103636727936367280T-16GENIChomozygous51413812
103636733936367340TTGTTTG10GENIChomozygous51413819
103636738436367385AG13GENIChomozygous51413821
103636785036367851CT35GENIChomozygous52040299
103636795936367960GA28GENIChomozygous52040301
103637063936370640A-8GENIChomozygous51413829