chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124707886247078863GA24GENIChomozygous115343146
124707927147079272CT25GENIChomozygous115343148
124707954547079546AG21GENIChomozygous115343150
124707976947079770GC21GENIChomozygous115343153
124707977547079776TC20GENIChomozygous115397400
124708168747081688GA29GENIChomozygous115343155
124708199247081993CA24GENIChomozygous115343157
124708207447082075TC25GENIChomozygous115343159
124708222747082228AC21GENIChomozygous115397404
124708256247082563TC15GENIChomozygous115397406
124708289847082899TC26GENIChomozygous115343161
124708339947083400GA18GENIChomozygous115397408
124708350047083501CT22GENIChomozygous115343163
124708420447084205TC19GENIChomozygous115397410
124708510447085105GA22GENIChomozygous115343165
124708531147085312AT26GENIChomozygous115343167
124708612647086127CT15GENIChomozygous115343169
124708630747086308CT19GENIChomozygous115343171
124708759147087592GA18GENIChomozygous115343173
124708779847087799CT20GENIChomozygous115343175
124708978047089781CT22GENIChomozygous115343177
124709078247090783AG17GENIChomozygous115343179
124709326947093270TC15GENIChomozygous115343181
124709336247093363CA20GENICpossibly homozygous115343183
124709347547093476CT31GENIChomozygous115343185
124709425847094259TC16GENIChomozygous115343187
124707977147079772GC21GENIChomozygous115583591
124707979647079804GGAGGGAG19GENIChomozygous128996953
124708125347081253A16GENIChomozygous128996954
124708138347081383GCTACACAGCGAGTTCCAGGCCAGTGGT12GENIChomozygous128996955
124708943847089439T15GENIChomozygous128996956
124709129547091295A18GENIChomozygous128996957
124709314047093143CTA22GENIChomozygous128996958
124709360447093604CT16GENIChomozygous128996959
124709395847093958T22GENIChomozygous128996960
124708247947082480TC19GENIChomozygous118272559
124708641147086412TC16GENIChomozygous115452041
124708957547089576AG30GENIChomozygous115704627