chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104618280246182803AG15GENIChomozygous116877594
104618589246185893GA25GENIChomozygous116877596
104618698446186985CA28GENIChomozygous116877598
104618962646189627AG22GENIChomozygous116585224
104618469746184698CT21GENIChomozygous116585214
104618503546185036AG27GENIChomozygous116585218
104618575046185751TC30GENIChomozygous116585220
104618741246187413CA18GENIChomozygous116585222
104618457846184578T24GENIChomozygous128814161
104618848946188491CA23GENIChomozygous128814163
104618538346185384AG27GENIChomozygous117410415
104619034446190345AT17GENIChomozygous116877600
104619051546190516TC29GENIChomozygous116585226
104619458146194582TC26GENIChomozygous116585230
104619492246194923TG26GENIChomozygous116585232
104619529846195299GT19GENIChomozygous116585234
104619623846196238AAAAC20GENIChomozygous128814166
104620004846200049A24GENIChomozygous128814171
104620087146200872TG26GENIChomozygous116877602
104620111346201114AG23GENIChomozygous116585236
104620127946201280GA23GENIChomozygous116877604
104620286146202861CAGGGCTA23GENIChomozygous128814172
104620301746203018AG27GENIChomozygous116877606
104620373246203733TC21GENIChomozygous116585238
104620481346204814TG19GENIChomozygous116585240
104618969346189703TATATGTGTA26GENIChomozygous131092518
104619564946195651AC23GENIChomozygous131092519