chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124707886247078863GA19GENIChomozygous115343146
124707927147079272CT25GENIChomozygous115343148
124707954547079546AG24GENIChomozygous115343150
124707976947079770GC11GENIChomozygous115343153
124707977547079776TC11GENIChomozygous115397400
124707977147079772GC11GENIChomozygous115583591
124708168747081688GA18GENIChomozygous115343155
124708199247081993CA22GENIChomozygous115343157
124708207447082075TC24GENIChomozygous115343159
124708222747082228AC12GENIChomozygous115397404
124708247947082480TC11GENIChomozygous118272559
124708256247082563TC12GENIChomozygous115397406
124708289847082899TC12GENIChomozygous115343161
124708339947083400GA17GENIChomozygous115397408
124708350047083501CT12GENIChomozygous115343163
124708380247083802TCA18GENIChomozygous132707324
124708420447084205TC11GENIChomozygous115397410
124708510447085105GA8GENIChomozygous115343165
124708531147085312AT14GENIChomozygous115343167
124708612647086127CT13GENIChomozygous115343169
124708630747086308CT8GENIChomozygous115343171
124708759147087592GA14GENIChomozygous115343173
124708779847087799CT11GENIChomozygous115343175
124708978047089781CT11GENIChomozygous115343177
124709078247090783AG16GENIChomozygous115343179
124709326947093270TC11GENIChomozygous115343181
124709336247093363CA14GENIChomozygous115343183
124709347547093476CT9GENIChomozygous115343185
124709395847093958T12GENIChomozygous128996960
124708138347081383GCTACACAGCGAGTTCCAGGCCAGTGGT16GENIChomozygous128996955
124707979647079804GGAGGGAG11GENIChomozygous128996953
124708125347081253A18GENIChomozygous128996954
124708943847089439T7GENIChomozygous128996956
124709314047093143CTA17GENIChomozygous128996958
124709360447093604CT6GENIChomozygous128996959
124708641147086412TC11GENIChomozygous115452041
124708957547089576AG17GENIChomozygous115704627
124709425847094259TC13GENIChomozygous115343187