chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104651515746515158TC19GENIChomozygous116586180
104651906246519063TC13GENIChomozygous116586182
104651906346519064TC13GENIChomozygous117058728
104652163146521632GA24GENIChomozygous116586184
104652445946524460CT21GENIChomozygous116586186
104653048546530486AG13GENIChomozygous116586188
104653075046530751CA16GENIChomozygous116586190
104653571446535715TC20GENIChomozygous116586192
104653614246536143TC16GENIChomozygous116772764
104653692446536925AT13GENIChomozygous116586194
104653705946537060CT19GENIChomozygous116586196
104653718146537182TC21GENIChomozygous116586198
104653798446537985TC14GENIChomozygous116586200
104654140046541401AG9GENIChomozygous116586202
104654179046541791TC22GENIChomozygous116586204
104654377746543778CT15GENIChomozygous116586206
104655157346551574GC13GENIChomozygous116586212
104655464746554648CA13GENIChomozygous116586214
104655583146555832CA18GENIChomozygous116586216
104656156446561565TC4GENIChomozygous116586218
104656349846563499CT14GENIChomozygous116772770
104656490446564905AG14GENIChomozygous116586220
104656561246565613GT26GENIChomozygous116586222
104656614846566149TC18GENIChomozygous116586224
104656630746566308GA14GENIChomozygous116586226
104656695046566951CA14GENIChomozygous116586228
104656749546567496CT13GENIChomozygous116586230
104656764346567644CT9GENIChomozygous116586232
104656804146568042AG9GENIChomozygous116586234
104656822046568221CG14GENIChomozygous116586236
104656824146568242CT19GENIChomozygous116586238
104656861246568613GT19GENIChomozygous116586240
104656869846568699GA7GENIChomozygous116586242
104656877346568774CT9GENIChomozygous116586244
104656892646568927TC23GENIChomozygous116586246
104656894746568948AC22GENIChomozygous116586248
104656932046569321CT24GENIChomozygous116586250
104656940146569402TC20GENIChomozygous116586252