chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1275040142275040143GA13GENIChomozygous595019459
1275040201275040202GA9GENIChomozygous595019460
1275040748275040749TTAAG22GENIChomozygous724380121
1275040749275040750TTC22GENIChomozygous724380122
1275041127275041128CCT26GENICpossibly homozygous724380123
1275041438275041439GA45GENIChomozygous592864241
1275041441275041442TC46GENIChomozygous592864242
1275041720275041721CA31GENIChomozygous592864243
1275043461275043469TTTTTTTT--------17GENICheterozygous724380126
1275043464275043469TTTTT-----17GENICheterozygous724380127
1275044096275044097CT23GENIChomozygous595019461
1275044321275044333TGTGTGTGTGTG------------7GENIChomozygous724380130
1275044563275044564GGCACA12GENIChomozygous724380132
1275044681275044683AC--21GENIChomozygous724380137
1275045373275045374CCTTTTT22GENIChomozygous724380140
1275045702275045703CT29GENIChomozygous592864244
1275045961275045962AG37GENIChomozygous592864245
1275046245275046246TC32GENIChomozygous592864246
1275046776275046777C-31GENIChomozygous724380141
1275047116275047117GA21GENIChomozygous592864247
1275047239275047240CA36GENIChomozygous595019462
1275048193275048195CG--28GENIChomozygous724380142
1275048287275048288AG23GENIChomozygous592864248
1275048349275048352CTG---25GENIChomozygous724380143
1275049325275049326CCT10GENICheterozygous724380144