chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108890271588902716GA29GENIChomozygous51536281
108890363088903631GA30GENIChomozygous51536282
108890545188905452CT31GENIChomozygous51925201
108890557788905580TTG---22GENIChomozygous51536283
108890618688906187TA34GENIChomozygous51536284
108890642888906429GA27GENIChomozygous51536285
108890823588908236TC31GENIChomozygous51536286
108890935488909355GGT28GENIChomozygous51536289
108891122988911237CACACACA--------2GENICheterozygous53076833
108891123188911237CACACA------2GENICheterozygous53076835
108891158588911586GA27GENIChomozygous51536293
108891192388911924CCT7GENICheterozygous51536294
108891282888912829AC29GENIChomozygous51536295
108891305688913057AG21GENIChomozygous51536296
108891370888913709TC38GENIChomozygous51536297
108891399788913998CT37GENIChomozygous51536298
108891414688914147AAG17GENIChomozygous51536299
108891429788914298AG16GENIChomozygous51536300
108891475088914751CT13GENIChomozygous52809096
108891475288914753CT14GENIChomozygous52809099
108891475488914755CT15GENIChomozygous52809102
108891475588914756CG15GENIChomozygous52809105
108891479488914795GGTGTGTC30GENICpossibly homozygous52809108
108891480388914804CT30GENICpossibly homozygous51536307
108891543388915434CT35GENIChomozygous51536308
108891544588915446AG32GENIChomozygous51536309
108891583388915837TTTG----10GENIChomozygous51536310
108891683888916839GGA19GENICpossibly homozygous51536312
108891731088917311TG17GENICpossibly homozygous51536313
108891735288917353AG11GENIChomozygous51536314
108891796888917969TA20GENIChomozygous51925203
108891836888918369A-24GENIChomozygous51536315
108891885788918858AACC26GENIChomozygous51536317
108891891288918913CA27GENIChomozygous51925205
108892345888923459TTA23GENIChomozygous51925207
108892431688924317TC36GENIChomozygous51536327
108892490388924905GA--13GENICheterozygous51536328
108893549388935494CCCACACACACACACA6GENIChomozygous52683450
108893768488937685A-19GENICheterozygous52322991