chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147537020147537021G12GENIChomozygous128253750
5147537115147537115CC29GENIChomozygous128253751
5147537136147537137T28GENIChomozygous128253752
5147537153147537154GA29GENIChomozygous114046166
5147537162147537162A30GENIChomozygous128253753
5147537164147537164A30GENIChomozygous128253754
5147537201147537201T27GENIChomozygous128253755
5147537211147537212GT27GENIChomozygous114046167
5147537223147537224A26GENIChomozygous128253756
5147537355147537356A31GENIChomozygous128253757
5147537362147537364TT31GENIChomozygous128253758
5147537377147537377T31GENIChomozygous128253759
5147537393147537394A27GENIChomozygous128253760
5147537414147537415T24GENIChomozygous128253761
5147537423147537423T24GENIChomozygous128253762
5147537433147537433T26GENIChomozygous128253763
5147537435147537439TCTC27GENIChomozygous128253764
5147537471147537471C23GENIChomozygous128253765
5147537486147537486C19GENIChomozygous128253766
5147537503147537503G23GENIChomozygous128253767
5147537505147537505T24GENIChomozygous128253768
5147537544147537545T26GENIChomozygous128253769
5147537684147537685CT27GENIChomozygous114046171
5147538543147538544GA23GENICpossibly homozygous114046173
5147540579147540580AG23GENIChomozygous114046175
5147540591147540592AG20GENIChomozygous114046177
5147541272147541273GA24GENIChomozygous114046179
5147541520147541521TG19GENIChomozygous114046181
5147541547147541548CG19GENIChomozygous114046183
5147541931147541932AG18GENIChomozygous114046185
5147541939147541940AG17GENIChomozygous114046187
5147542325147542326T12GENIChomozygous128253770
5147542451147542452AG8GENIChomozygous114046189
5147542484147542485CG9GENIChomozygous114046191
5147543257147543258TC7GENICpossibly homozygous114046193
5147543336147543336C14GENICpossibly homozygous128253771
5147543872147543873CT25GENIChomozygous114046195
5147544730147544731AG9GENIChomozygous114046197
5147544904147544905CT22GENIChomozygous114046199
5147546105147546106TC17GENIChomozygous114046201