chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
114191128641911287AT15GENIChomozygous115843848
114191633941916340GA10GENIChomozygous116306192
114196614541966146CG12GENIChomozygous115844128
114196951441969515CG10GENIChomozygous115844162
114197015341970154CA8GENIChomozygous115844166
114197025941970260CT6GENIChomozygous115844168
114196922441969225AG12GENIChomozygous115962566
114205786742057868CA21GENIChomozygous116306193
114205978842059789TG16GENIChomozygous116306194
114219984642199847GA16GENICheterozygous116306195
114219984842199849CT16GENICheterozygous116306196
114220771042207711CA21GENIChomozygous116130684
114220771142207712AC21GENIChomozygous116306197
114220781842207819AC6GENIChomozygous115962572
114220784242207843AT4GENIChomozygous116306198
114221047342210474AG24GENIChomozygous115844928
114221047542210476GT22GENIChomozygous115844930
114221052242210523TA23GENIChomozygous115844932
114221066242210663CG14GENIChomozygous115844933
114221075742210758TA10GENIChomozygous115962573
114221075842210759AT10GENIChomozygous115962574
114223923442239235CA17GENIChomozygous115845015
114223929542239296AG15GENIChomozygous115845017
114223929842239299CA15GENIChomozygous115845019
114223939542239396GC21GENIChomozygous115962577
114225006842250069GT15GENIChomozygous115845119
114226581242265813AC11GENIChomozygous116306199
114226581942265820GA12GENIChomozygous116306200
114226582042265821AG12GENIChomozygous116306201
114234314842343149AG21GENIChomozygous115845270
114234355242343553GA18GENIChomozygous116306202
114254082542540826TG22GENIChomozygous115845940
114268901042689011CA25GENIChomozygous115962582
114268901142689012AT26GENIChomozygous115962583
114282221642822217GT9GENIChomozygous116184861
114282221842822219GT9GENIChomozygous116184863
114282222042822221GT10GENICpossibly homozygous116233690
114283922842839229GC35GENIChomozygous115846682