chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41418139714181398TG4GENIChomozygous56759722
41418140014181401CT4GENIChomozygous56759723
41418323014183232CG--2GENIChomozygous56759724
41418348414183489TGACT-----4GENICheterozygous56759727
41418361814183619CA6GENIChomozygous56759729
41418362414183625TC5GENIChomozygous56759730
41418370114183702GC2GENIChomozygous56759731
41418375214183753GT4GENIChomozygous56759733
41418377214183773GA5GENIChomozygous56759734
41418394014183941A-8GENIChomozygous56759735
41418396514183966CT9GENIChomozygous56759736
41418434914184350TG9GENIChomozygous56759737
41418494714184948AG4GENIChomozygous56759740
41418496114184962GC4GENIChomozygous56759741
41418504614185047AC5GENIChomozygous56759742
41418582114185822CT16GENICheterozygous56759743
41418583414185835G-18GENICheterozygous58274854
41418585514185859GAAA----19GENICheterozygous58274856
41418610314186104TTA3GENIChomozygous56759748
41418615914186160GGAA1GENIChomozygous56759751
41418708614187087TC10GENIChomozygous56759758
41418509414185100AATAAT------4GENIChomozygous58452626
41418593314185942TCTAAGAAG---------8GENICheterozygous58328079
41418596414185965AATG11GENICheterozygous58328080
41418596814185969AATGTTCTCACTTC10GENICheterozygous58328081
41418739914187400T-23GENICheterozygous56759772
41418758114187582TTTA8GENICpossibly homozygous58452628
41418808814188089TTA3GENICheterozygous58328084
41418912514189126GGA2GENICheterozygous58404272
41419347214193473A-1GENIChomozygous56759800
41419548714195488AG9GENIChomozygous56759801
41419554014195541GGA5GENIChomozygous56759802
41420373614203737GA1GENIChomozygous56759804
41420379414203795GGA3GENIChomozygous56759805
41421074414210745CG5GENIChomozygous56759809
41421085114210852CG7GENIChomozygous56759810
41421692314216924CCT3GENIChomozygous58328090
41421697014216975TTTTT-----9GENIChomozygous58328091