chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105645877856458779AG59GENIChomozygous116783560
105645889356458894AG70GENIChomozygous116783562
105645889956458900AG69GENIChomozygous116783564
105645926856459269AG58GENIChomozygous116783566
105645934456459345AG60GENIChomozygous116783568
105646093656460937GA46GENIChomozygous117059716
105646180156461802GT48GENIChomozygous116783572
105646185456461855TG40GENIChomozygous116783574
105646294856462949GA40GENIChomozygous117059718
105646301956463020GA56GENIChomozygous117059720
105646323556463236AG45GENIChomozygous116783576
105646368056463681AG42GENIChomozygous117059722
105646369856463699TC40GENIChomozygous116783578
105646406056464061TC53GENIChomozygous116783580
105646477356464774AG54GENIChomozygous116783582
105646624156466242GA45GENIChomozygous117059724
105646642756466428CT45GENIChomozygous117059726
105646651156466512GA38GENIChomozygous116935327
105646739656467397GA68GENIChomozygous116783584
105646779356467794GC69GENIChomozygous116935329
105647023056470231AG51GENIChomozygous116935333
105647106856471069AG59GENIChomozygous116935335
105647157856471579TC41GENIChomozygous116783590
105647253756472538TC43GENIChomozygous116935339
105647255256472553AG40GENIChomozygous116783592
105646201656462017GC22GENIChomozygous117218772
105646609856466099GC16GENICheterozygous132883061
105646269256462694TA46GENIChomozygous131094500
105646201556462015AGA23GENIChomozygous128819232
105646199956461999C25GENIChomozygous128819230
105646200856462014TCTTAT23GENIChomozygous128819231
105646458756464587GAAG35GENIChomozygous131094501
105646939756469397T37GENIChomozygous131094502
105646989356469893AC39GENIChomozygous131094503
105647212356472123C40GENICpossibly homozygous131094504
105647276756472767TATATAG29GENIChomozygous131094505
105646609456466095GC26GENIChomozygous131101414
105646609656466097GC15GENICheterozygous132696396