chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
174400130944001310AC14GENIChomozygous47113498
174400192244001923GA29GENIChomozygous47113499
174400237444002375AG43GENIChomozygous47113500
174400243744002550ATTGGACTACAGGGAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAGAACCAAAAAAA-----------------------------------------------------------------------------------------------------------------42GENIChomozygous47709016
174400330944003310AC26GENIChomozygous47113501
174400436544004366AG26GENIChomozygous47113502
174400483644004837GA22GENIChomozygous47113503
174400500644005007AG28GENIChomozygous47113504
174400578144005782TC18GENIChomozygous47113505
174400635544006356AG29GENIChomozygous47113506
174400697044006971CT24GENIChomozygous47113511
174400766844007669AG24GENIChomozygous47113512
174400775244007753TTC17GENIChomozygous47113513
174400931544009316GT23GENIChomozygous47113514
174401099744010998CT25GENIChomozygous47113515
174401110344011104GGGT9GENICheterozygous47113516
174401141244011413TC37GENIChomozygous47113517
174401264944012653TTTT----24GENIChomozygous47113519
174401353744013538AG31GENIChomozygous47113520
174401378544013786GA44GENIChomozygous47113521
174401388444013885GA34GENIChomozygous47113522
174401723444017235TC31GENIChomozygous47113523
174401874544018746GA22GENIChomozygous47113524
174401996844019969TC27GENIChomozygous47113526
174402056644020570ACAC----14GENICpossibly homozygous47113527
174402328744023288CG30GENIChomozygous47113528
174402422244024223CT23GENIChomozygous47113530
174402531244025313AG21GENIChomozygous47113531
174402557244025573CCTCTGAAAATAAGCATTTT11GENIChomozygous47739396
174400680544006806CCACACA5GENIChomozygous47325769
174400681744006819CC--4GENIChomozygous47739388
174400961544009629ACACACACACACAC--------------16GENIChomozygous47739392
174401190944011910CCGATAGATA10GENIChomozygous47739394
174402568544025686CCT12GENICpossibly homozygous47113532
174402712444027125TG26GENIChomozygous47113533