chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107087451770874518TA26GENICheterozygous118042998
107087451970874520TA25GENICheterozygous118042999
107087452170874522TA25GENICheterozygous118043000
107087452370874524TA25GENICheterozygous116628811
107087685570876856TC80GENIChomozygous116628825
107087711670877117CT34GENICpossibly homozygous118043001
107087767570877676TG49GENICpossibly homozygous118043002
107087799170877992AT55GENICpossibly homozygous116628855
107087818570878186CT75GENICpossibly homozygous116628859
107088139470881395TC50GENIChomozygous118043003
107088142170881422TC47GENIChomozygous118043004
107088146370881464TC51GENIChomozygous116628883
107088227370882274AG58GENIChomozygous116799610
107088240070882401CT61GENIChomozygous117131002
107088244670882447CT43GENIChomozygous117131003
107088388270883883CT75GENIChomozygous117131005
107088406270884063AG58GENIChomozygous116628889
107088432670884327CT56GENIChomozygous117131006
107088449770884498GT42GENIChomozygous117131007
107088451270884513GT55GENIChomozygous118043005
107088478370884784TC59GENIChomozygous116628891
107088490670884907TG69GENIChomozygous117131008
107088506170885062AG56GENIChomozygous116628893
107088549570885496GA59GENICpossibly homozygous117131009
107088563270885633CA71GENICpossibly homozygous117131010
107088571170885712GT54GENIChomozygous116628897
107088591870885919AT32GENIChomozygous117131011
107088596070885961AG35GENIChomozygous116628899