chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105645877856458779AG72GENIChomozygous116783560
105645889356458894AG73GENIChomozygous116783562
105645889956458900AG72GENIChomozygous116783564
105645926856459269AG64GENIChomozygous116783566
105645934456459345AG63GENIChomozygous116783568
105646093656460937GA70GENIChomozygous117059716
105646180156461802GT33GENIChomozygous116783572
105646185456461855TG32GENIChomozygous116783574
105646199956461999C8GENIChomozygous128819230
105646200856462014TCTTAT8GENIChomozygous128819231
105646201556462015AGA8GENIChomozygous128819232
105646201656462017GC10GENIChomozygous117218772
105646269256462694TA37GENICpossibly homozygous131094500
105646294856462949GA60GENIChomozygous117059718
105646301956463020GA69GENIChomozygous117059720
105646323556463236AG51GENIChomozygous116783576
105646368056463681AG59GENIChomozygous117059722
105646369856463699TC64GENIChomozygous116783578
105646406056464061TC72GENIChomozygous116783580
105646458756464587GAAG45GENIChomozygous131094501
105646477356464774AG71GENICpossibly homozygous116783582
105646624156466242GA60GENIChomozygous117059724
105646642756466428CT55GENIChomozygous117059726
105646651156466512GA70GENIChomozygous116935327
105646739656467397GA73GENIChomozygous116783584
105646779356467794GC77GENIChomozygous116935329
105646939756469397T44GENICpossibly homozygous131094502
105646989356469893AC48GENIChomozygous131094503
105647023056470231AG43GENIChomozygous116935333
105647106856471069AG64GENIChomozygous116935335
105647157856471579TC64GENIChomozygous116783590
105647212256472122AC49GENICheterozygous132692169
105647212356472123C49GENICpossibly homozygous131094504
105647253756472538TC82GENIChomozygous116935339
105647255256472553AG75GENIChomozygous116783592
105647276756472767TATATAG42GENIChomozygous131094505