chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1275040748275040749TTAAG17GENIChomozygous61228822
1275040749275040750TTC17GENIChomozygous61228823
1275040879275040887AACAATTA--------19GENIChomozygous61972510
1275040889275040890AC18GENIChomozygous61972511
1275041127275041128CCT26GENIChomozygous61228824
1275041484275041485GC16GENIChomozygous61647603
1275041720275041721CA18GENIChomozygous61228827
1275041746275041747CT25GENIChomozygous61972512
1275043460275043469TTTTTTTTT---------5GENICheterozygous61228828
1275043461275043469TTTTTTTT--------5GENICheterozygous62280897
1275044096275044097CT16GENIChomozygous61228830
1275044312275044313CCTGTG1GENIChomozygous62251525
1275044681275044683AC--9GENIChomozygous61228832
1275045374275045377TTT---8GENICheterozygous61972513
1275045702275045703CT13GENIChomozygous61228833
1275045961275045962AG10GENIChomozygous61228834
1275046245275046246TC12GENIChomozygous61228835
1275046776275046777C-11GENIChomozygous61228836
1275047116275047117GA18GENIChomozygous61228837
1275047445275047446CT22GENIChomozygous61972514
1275047940275047941CT19GENIChomozygous61972515
1275048193275048195CG--12GENIChomozygous61228839
1275048287275048288AG12GENIChomozygous61228840
1275048917275048918AT25GENIChomozygous61647612
1275049205275049206CT11GENIChomozygous61972516
1275049269275049270AAGTTT16GENIChomozygous61647613
1275049320275049321CG8GENIChomozygous61647614
1275049325275049326CCTTTT3GENIChomozygous61684643
1275049610275049611AAACC19GENIChomozygous61335346
1275049867275049868CT7GENIChomozygous61647616
1275044563275044564GGCACACACACACACACACA2GENIChomozygous62218018