chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1228737670228737671AG30GENIChomozygous525021216
1228739709228739710AG29GENIChomozygous528049582
1228739864228739868CCCC----16GENIChomozygous691860154
1228741235228741236GT22GENIChomozygous528049583
1228741277228741278T-11GENICheterozygous691860155
1228741329228741330AAGAGAG9GENIChomozygous691860156
1228741505228741506A-11GENIChomozygous691860157
1228741525228741526A-7GENIChomozygous691860158
1228741819228741820CCG24GENIChomozygous691860159
1228744220228744221TC38GENIChomozygous528049584
1228745418228745419CT34GENIChomozygous528049585
1228746722228746723TC26GENIChomozygous528049586
1228747028228747043CTGGCATTGTGGTAG---------------10GENIChomozygous691860160
1228751732228751733CCATTT13GENIChomozygous691860161
1228752487228752488AG37GENIChomozygous528049587
1228752836228752837G-31GENIChomozygous691860162
1228753035228753036CCCACA10GENICpossibly homozygous691860163
1228753085228753089ACAC----13GENICpossibly homozygous691860164
1228753087228753089AC--13GENICheterozygous691860165
1228754008228754009T-28GENIChomozygous691860166
1228754121228754122AG36GENICheterozygous528049588
1228755144228755145CT22GENIChomozygous528049589
1228755467228755468GGCA24GENICpossibly homozygous691860167
1228755487228755488TTAC27GENICheterozygous691860168
1228755487228755488TTACAC27GENICpossibly homozygous691860169
1228756439228756440CCT8GENICheterozygous691860170
1228756440228756441T-8GENICheterozygous691860171
1228756521228756522AAGT9GENICheterozygous691860172