chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
181567699515676999CCCC----28GENIChomozygous46575453
181567851715678518CT39GENIChomozygous46575455
181567878915678790CA25GENIChomozygous46575456
181567959215679593T-25GENIChomozygous46575457
181568007315680074AAT14GENICpossibly homozygous46575458
181568071715680718GA18GENIChomozygous46575459
181568104115681042CCA19GENICheterozygous46368146
181568104215681043A-19GENICheterozygous46841373
181568138615681387CA27GENIChomozygous46575460
181568176715681874CCAAGAACTGTGTATGTTTTTTTTTCTTTTTTTTCGGAACTGGGGACCGAACCCAGGGCCTTGCGGTTGCTAGGCAAGCACTCTACCTCTGAGCCAAATCCCCAACC-----------------------------------------------------------------------------------------------------------19GENIChomozygous46792114
181568206115682062CT20GENIChomozygous46575461
181568230615682307GA18GENIChomozygous46575462
181568294415682945AC27GENIChomozygous46575463
181568373015683731A-33GENIChomozygous46575464
181568452115684522GA11GENIChomozygous46575465
181568518715685188CCTGT31GENIChomozygous46575466
181568548515685486A-36GENICpossibly homozygous46575467
181568567715685678TC29GENIChomozygous46575468
181568623515686236TC33GENIChomozygous46575469
181568665715686658GA10GENIChomozygous46575470