chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
44490869444908695CT20GENIChomozygous112620746
44490879544908796AG20GENIChomozygous112620748
44490887844908879TC31GENIChomozygous112620750
44490946344909464AG22GENIChomozygous112620752
44491055444910555CT13GENIChomozygous112620754
44491082744910828AG5GENIChomozygous112620756
44491201744912018GA12GENIChomozygous112620758
44491213144912132GT18GENIChomozygous112620760
44491299944913000TC20GENIChomozygous112620766
44491305444913055TC15GENICpossibly homozygous112620768
44491453544914536CT8GENIChomozygous112620772
44491472644914727GC19GENIChomozygous112620774
44491533044915331AG12GENIChomozygous112620776
44491714344917144GA27GENIChomozygous112620778
44491817044918171GA26GENIChomozygous112620782
44491898444918985CG12GENIChomozygous112620784
44491969644919697AG6GENIChomozygous112620786
44491980144919802AT10GENIChomozygous112620788
44492020644920207CT18GENIChomozygous112620789
44492082044920821AG8GENIChomozygous112620791
44492141444921415GA20GENIChomozygous112620793
44492153544921536CA7GENIChomozygous112620795
44492189744921898GC7GENIChomozygous112620797
44493107444931075AG10GENIChomozygous112620809
44493236244932363TC3GENIChomozygous112620811
44493353444933535TC12GENIChomozygous112620813
44493363644933637GA10GENIChomozygous112620815
44493383444933835TC19GENIChomozygous112620817
44493423144934232GA14GENIChomozygous112620819
44493522244935223CT12GENIChomozygous112620821