chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107087225670872257CT10GENIChomozygous117130998
107087685570876856TC22GENIChomozygous116628825
107087799170877992AT37GENIChomozygous116628855
107088103970881040GA25GENIChomozygous117130999
107088146370881464TC25GENIChomozygous116628883
107088169870881699TG29GENIChomozygous117131000
107088221070882211GA14GENIChomozygous117131001
107088227370882274AG12GENIChomozygous116799610
107088240070882401CT29GENICpossibly homozygous117131002
107088244670882447CT22GENIChomozygous117131003
107088368270883683CT16GENIChomozygous117131004
107088388270883883CT25GENIChomozygous117131005
107088406270884063AG31GENIChomozygous116628889
107088432670884327CT24GENIChomozygous117131006
107088449770884498GT21GENIChomozygous117131007
107088478370884784TC22GENIChomozygous116628891
107088490670884907TG22GENIChomozygous117131008
107088506170885062AG26GENIChomozygous116628893
107088549570885496GA29GENIChomozygous117131009
107088563270885633CA22GENIChomozygous117131010
107088571170885712GT21GENIChomozygous116628897
107088591870885919AT25GENIChomozygous117131011
107088596070885961AG19GENIChomozygous116628899