chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117274995072749951AG22GENIChomozygous116052794
117275006772750068TA28GENIChomozygous115987547
117275048772750488TG23GENIChomozygous116105831
117275068772750688GC22GENIChomozygous116105832
117275126072751261TG27GENIChomozygous115899864
117275198672751987TC7GENIChomozygous118195681
117275500772755008GA38GENIChomozygous115899870
117282440972824410AG4GENIChomozygous118195682
117282455072824551AG10GENIChomozygous118163992
117282455372824554TG10GENIChomozygous118195683
117282464072824641AT3GENIChomozygous118163993
117282495272824953AG37GENIChomozygous116161721
117282501572825016CT18GENIChomozygous116110601
117282508572825086GA20GENIChomozygous116110602
117282679072826791TC20GENIChomozygous118195684
117283400772834008GA13GENIChomozygous118195685
117284795172847952TC19GENIChomozygous118195686
117284991972849920AC14GENIChomozygous118195687
117285008372850084CA16GENIChomozygous118195688
117289941972899420AG19GENIChomozygous118195689
117291152972911530CA14GENIChomozygous118195690
117300043673000437GT16GENIChomozygous118163994
117301927273019273TA5GENIChomozygous116052800
117302454273024543GC26GENIChomozygous115987559
117301932573019326CT4GENICheterozygous118195691
117301935973019360TC7GENICheterozygous116397590
117301953473019535AG12GENIChomozygous115987553
117302464473024645CT36GENIChomozygous116105833
117302475273024753TC24GENIChomozygous116105834
117302513073025131CT31GENIChomozygous116105835
117302601073026011GA22GENIChomozygous116105836
117302689873026899GA33GENIChomozygous116105837
117302739073027391CT18GENIChomozygous116105838
117302789973027900TC18GENIChomozygous116105839
117302845573028456TC20GENIChomozygous115987565
117302870673028707GA21GENIChomozygous116105840
117302960673029607CA5GENIChomozygous116161725
117302988073029881AT25GENIChomozygous116161727
117303128273031283TG32GENICpossibly homozygous115987567
117303386873033869TC20GENIChomozygous115987569
117303418873034189CT23GENICpossibly homozygous118195692