chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174400130944001310AC26GENIChomozygous47113498
174400192244001923GA23GENIChomozygous47113499
174400237444002375AG26GENIChomozygous47113500
174400330944003310AC14GENIChomozygous47113501
174400361944003620CT22GENIChomozygous47419469
174400413544004136TC25GENIChomozygous47419471
174400483644004837GA30GENIChomozygous47113503
174400500644005007AG26GENIChomozygous47113504
174400578144005782TC20GENIChomozygous47113505
174400635544006356AG29GENIChomozygous47113506
174400679944006806CACACAC-------17GENICpossibly homozygous47113507
174400680544006806C-17GENIChomozygous47113508
174400680544006806CCA2GENICheterozygous47113509
174400680544006806CCACACA2GENICheterozygous47325769
174400681544006818CCC---14GENIChomozygous47325771
174400766844007669AG27GENIChomozygous47113512
174400775244007753TTC29GENIChomozygous47113513
174400931544009316GT22GENICpossibly homozygous47113514
174401099744010998CT18GENIChomozygous47113515
174401110344011104GGGT11GENICheterozygous47113516
174401141244011413TC21GENIChomozygous47113517
174401196044011961TC30GENICpossibly homozygous47419473
174401196444011965TC31GENIChomozygous47419475
174401264944012653TTTT----16GENIChomozygous47113519
174401353744013538AG20GENIChomozygous47113520
174401378544013786GA19GENIChomozygous47113521
174401723444017235TC20GENIChomozygous47113523
174401974744019748CCT20GENIChomozygous47419477
174401996844019969TC37GENIChomozygous47113526
174402056644020570ACAC----1GENIChomozygous47113527
174402134744021348GA22GENIChomozygous47419479
174402328744023288CG33GENIChomozygous47113528
174402531244025313AG12GENIChomozygous47113531
174402568544025686CCT6GENIChomozygous47113532