chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176162966361629664CT25GENIChomozygous140156960
176162983861629839GT8GENIChomozygous140156961
176162986061629861CA8GENIChomozygous140156962
176163008961630093ACAC13GENIChomozygous140031524
176163009561630105GGAAAGAAAC14GENIChomozygous140031525
176163027661630277TA23GENIChomozygous140156963
176163072361630724TC19GENIChomozygous140156964
176163093361630933A17GENIChomozygous140031526
176163112461631130ATATAC15GENIChomozygous140031527
176163193661631936GTACCTGGTGCCCTG20GENIChomozygous140031528
176163254261632542GCC16GENIChomozygous140031529
176163254461632544A17GENIChomozygous140031530
176163267861632679C21GENIChomozygous403668579
176163111961631120TC17GENIChomozygous155032053
176163111961631120T17GENICheterozygous403668575
176163267061632671C22GENIChomozygous403668576
176163267061632671CA22GENICheterozygous403668577
176163267061632671CG22GENICheterozygous403668578
176163267861632679CG21GENICheterozygous403668580
176163274661632755TAGCCTGTC22GENIChomozygous140031531
176163275861632759CG23GENIChomozygous140156965
176163313361633133A15GENICpossibly homozygous140031532
176163368661633687GA26GENIChomozygous140156966
176163509661635097AG12GENIChomozygous140156967
176163515561635155T9GENICpossibly homozygous140031533
176163541161635412CT17GENIChomozygous140156968
176163541461635415TC17GENIChomozygous140156969
176163569061635691A6GENIChomozygous403418860
176163569061635691AG6GENICheterozygous403418859
176163569261635693AG6GENICheterozygous403418861
176163569261635693A6GENIChomozygous403418862
176163569861635699AG6GENIChomozygous403418863
176163569861635699A6GENICheterozygous403418864
176163570061635701AG6GENIChomozygous403418865
176163570061635701A6GENICheterozygous403418866
176163583161635832AG6GENIChomozygous140156970
176163699861636999GC27GENIChomozygous140156971
176163700561637006AG29GENIChomozygous140156972