chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2217530778217530779AG35GENIChomozygous509679431
2217531441217531442CT43GENIChomozygous509679432
2217531761217531762CT74GENIChomozygous507900970
2217531850217531851CT61GENICpossibly homozygous507900971
2217531938217531939CCAAAA19GENICheterozygous685334562
2217531938217531939CCA19GENICheterozygous685334563
2217533101217533102AT37GENIChomozygous509679433
2217533487217533488CCT18GENICheterozygous685334564
2217533487217533488CCTT18GENICheterozygous685334565
2217534422217534423TG62GENICpossibly homozygous507900972
2217535148217535149TC58GENIChomozygous507900973
2217535275217535276GC68GENIChomozygous509679434
2217535389217535390TC31GENIChomozygous509679435
2217536071217536072TC51GENIChomozygous509679436
2217536085217536086AG57GENIChomozygous509679437
2217536086217536087GA57GENIChomozygous509679438
2217536385217536388TTT---28GENICpossibly homozygous685334566
2217536586217536587CCGTGTGT22GENIChomozygous685334567
2217536836217536837CT68GENIChomozygous509679439
2217536923217536924CT71GENIChomozygous509679440
2217537424217537425TC57GENIChomozygous507900974
2217538354217538355GA64GENIChomozygous509679441
2217540938217540939TC55GENIChomozygous509679442
2217541440217541441CCT36GENIChomozygous685334568
2217541453217541454GGT38GENIChomozygous685334569
2217542272217542273TC53GENIChomozygous507900975
2217542661217542662AG52GENIChomozygous509679443
2217543304217543305AT41GENIChomozygous509679444
2217543447217543448TG67GENICpossibly homozygous509679445
2217546112217546113GT58GENICpossibly homozygous507900976
2217546433217546434AAT86GENIChomozygous685334570
2217546841217546842T-59GENIChomozygous685334571