chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104618280246182803AG15GENIChomozygous116877594
104618379846183799GA4GENICheterozygous134491449
104618380046183801GA4GENICheterozygous134491450
104618380146183802TA3GENICheterozygous134491451
104618538346185384AG10GENIChomozygous117410415
104618575046185751TC18GENIChomozygous116585220
104618469746184698CT11GENIChomozygous116585214
104618503546185036AG17GENIChomozygous116585218
104618457846184578T17GENIChomozygous128814161
104618589246185893GA12GENIChomozygous116877596
104618698446186985CA23GENIChomozygous116877598
104618741246187413CA17GENIChomozygous116585222
104618848946188491CA25GENIChomozygous128814163
104618962646189627AG17GENIChomozygous116585224
104619034446190345AT17GENIChomozygous116877600
104619051546190516TC16GENIChomozygous116585226
104619458146194582TC25GENIChomozygous116585230
104619492246194923TG16GENIChomozygous116585232
104619529846195299GT17GENIChomozygous116585234
104619623846196238AAAAC16GENIChomozygous128814166
104619751146197513AG19GENICheterozygous128814170
104620004846200049A10GENIChomozygous128814171
104620087146200872TG17GENIChomozygous116877602
104620111346201114AG15GENIChomozygous116585236
104620127946201280GA24GENIChomozygous116877604
104620286146202861CAGGGCTA13GENIChomozygous128814172
104620301746203018AG22GENIChomozygous116877606
104620373246203733TC10GENIChomozygous116585238
104620481346204814TG12GENIChomozygous116585240
104618969346189703TATATGTGTA16GENIChomozygous131092518
104619564946195651AC20GENIChomozygous131092519