chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1275040748275040749T-14GENIChomozygous61228821
1275040748275040749TTAAG14GENIChomozygous61228822
1275040749275040750TTC14GENICpossibly homozygous61228823
1275040879275040887AACAATTA--------8GENIChomozygous61972510
1275040889275040890AC9GENIChomozygous61972511
1275041127275041128CCT14GENIChomozygous61228824
1275041720275041721CA30GENIChomozygous61228827
1275041746275041747CT24GENIChomozygous61972512
1275041484275041485GC29GENIChomozygous61647603
1275043460275043469TTTTTTTTT---------8GENICheterozygous61228828
1275044096275044097CT24GENIChomozygous61228830
1275044563275044564GGCACA12GENICheterozygous61228831
1275044590275044591TC47GENICheterozygous61335338
1275044681275044683AC--33GENIChomozygous61228832
1275045374275045377TTT---8GENIChomozygous61972513
1275045702275045703CT29GENIChomozygous61228833
1275045961275045962AG28GENIChomozygous61228834
1275046245275046246TC21GENIChomozygous61228835
1275046776275046777C-22GENIChomozygous61228836
1275047116275047117GA9GENIChomozygous61228837
1275047445275047446CT23GENIChomozygous61972514
1275047940275047941CT23GENIChomozygous61972515
1275048193275048195CG--25GENIChomozygous61228839
1275048287275048288AG35GENIChomozygous61228840
1275048917275048918AT26GENIChomozygous61647612
1275049205275049206CT31GENIChomozygous61972516
1275049269275049270AAGTTT19GENIChomozygous61647613
1275049320275049321CG14GENIChomozygous61647614
1275049325275049326CCTTTT4GENIChomozygous61684643
1275049533275049534A-4GENICheterozygous61228843
1275049610275049611AAACC19GENIChomozygous61335346
1275049867275049868CT32GENIChomozygous61647616