chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4171772847171772848C54GENIChomozygous128104787
4171772854171772854G53GENIChomozygous128104788
4171772857171772857C51GENIChomozygous128104789
4171772984171772984G56GENIChomozygous128104790
4171773045171773045AACAG45GENIChomozygous128104791
4171785380171785381T47GENIChomozygous128104792
4171789500171789500CCTGTG61GENIChomozygous128104793
4171793645171793679AAGCATGACAAGGTAGGAAGTGCCTTGCTTGGAG41GENIChomozygous128104794
4171802434171802435C58GENIChomozygous128104795
4171802475171802476A58GENIChomozygous128104796
4171808362171808416CGCACACACGCACGCGCGCGCGCGCGCGCACACACACACGCACGCGCGCGCGCG32GENICheterozygous128104797
4171815814171815815GA59GENIChomozygous112951993
4171816056171816057A48GENIChomozygous128104798
4171817326171817327TC23GENICpossibly homozygous113564057
4171820550171820551A11GENIChomozygous128104802
4171820564171820566GC13GENIChomozygous128104803
4171820585171820586T18GENIChomozygous128104804
4171820813171820814T20GENIChomozygous128104812
4171817623171817624TC35GENIChomozygous112952011
4171818116171818117CA51GENIChomozygous113314515
4171818648171818649AC43GENIChomozygous112952015
4171819520171819521CT44GENIChomozygous113314516
4171819598171819599AC51GENIChomozygous113314517
4171820138171820139GA49GENIChomozygous113314518
4171820540171820541AC10GENIChomozygous112952029
4171820600171820600C19GENIChomozygous128104805
4171820797171820797T14GENIChomozygous128104811
4171820858171820858C18GENIChomozygous128104813
4171820868171820868C22GENIChomozygous128104814
4171820878171820879AC25GENIChomozygous113067950
4171820882171820883AC27GENIChomozygous112952033
4171824314171824315AC55GENICpossibly homozygous112952049
4171824422171824423TC61GENICpossibly homozygous112952051
4171825366171825367TC57GENIChomozygous112952057
4171825617171825617G50GENIChomozygous128104816
4171825979171825980GA39GENIChomozygous112952061
4171826000171826001CT41GENIChomozygous113314519
4171826107171826108CT49GENIChomozygous112952063
4171820877171820878TA25GENIChomozygous119283200