chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44490869444908695CT28GENIChomozygous112620746
44490879544908796AG17GENIChomozygous112620748
44490887844908879TC28GENIChomozygous112620750
44490946344909464AG25GENIChomozygous112620752
44491055444910555CT22GENIChomozygous112620754
44491082744910828AG18GENIChomozygous112620756
44491201744912018GA26GENIChomozygous112620758
44491213144912132GT33GENIChomozygous112620760
44491299944913000TC28GENIChomozygous112620766
44491305444913055TC27GENIChomozygous112620768
44491416744914168AC21GENIChomozygous112620770
44491453544914536CT25GENIChomozygous112620772
44491472644914727GC28GENIChomozygous112620774
44491533044915331AG24GENIChomozygous112620776
44491714344917144GA21GENIChomozygous112620778
44491770344917704GA28GENIChomozygous112620780
44491817044918171GA27GENIChomozygous112620782
44491898444918985CG38GENIChomozygous112620784
44491980144919802AT23GENIChomozygous112620788
44492020644920207CT19GENIChomozygous112620789
44492082044920821AG38GENIChomozygous112620791
44492141444921415GA23GENIChomozygous112620793
44492153544921536CA24GENIChomozygous112620795
44492189744921898GC19GENIChomozygous112620797
44493063444930635GA16GENIChomozygous112620807
44493236244932363TC23GENIChomozygous112620811
44493353444933535TC13GENIChomozygous112620813
44493363644933637GA18GENIChomozygous112620815
44493383444933835TC21GENIChomozygous112620817
44493423144934232GA26GENIChomozygous112620819
44493522244935223CT21GENIChomozygous112620821