chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1160452255160452256CA17GENIChomozygous62841069
1160452672160452673TC16GENIChomozygous60916783
1160452911160452912TA18GENIChomozygous60916784
1160453819160453820CCA9GENIChomozygous60916786
1160455882160455883AC13GENIChomozygous62841070
1160457564160457565GA11GENIChomozygous60916793
1160457629160457630GA17GENIChomozygous62841071
1160459631160459632CA11GENIChomozygous60916799
1160460372160460373GA15GENIChomozygous60916802
1160453357160453358GA14GENIChomozygous61547154
1160463594160463595CT39GENIChomozygous60916805
1160463799160463800TC26GENIChomozygous60916806
1160464101160464102AG40GENIChomozygous60916807
1160465049160465050AG19GENIChomozygous61547162
1160465895160465896A-14GENIChomozygous60916810
1160465974160465975AG12GENIChomozygous62841072
1160467556160467557CG14GENIChomozygous60916814
1160467634160467638AGGA----7GENIChomozygous60916815
1160468189160468190GA22GENIChomozygous60916816
1160468223160468224TC20GENIChomozygous60916817
1160469251160469252CT13GENIChomozygous62577918
1160469507160469508AG22GENIChomozygous62841073
1160470256160470257GA20GENIChomozygous61547166
1160471040160471041CT16GENIChomozygous61547167
1160471521160471522AC29GENIChomozygous61547168
1160471681160471682T-14GENIChomozygous61547169
1160471690160471691GC15GENIChomozygous61547170
1160472034160472035CT19GENIChomozygous62841074
1160472271160472272CT18GENIChomozygous62841075
1160472435160472436AT21GENIChomozygous61547171
1160473004160473005GA19GENIChomozygous61547172
1160473167160473168CA14GENIChomozygous61547174