chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105645877856458779AG22GENIChomozygous116783560
105645889356458894AG27GENIChomozygous116783562
105645889956458900AG27GENIChomozygous116783564
105645926856459269AG20GENIChomozygous116783566
105645934456459345AG20GENIChomozygous116783568
105646093656460937GA18GENIChomozygous117059716
105646180156461802GT25GENIChomozygous116783572
105646185456461855TG23GENIChomozygous116783574
105646199956461999C11GENIChomozygous128819230
105646200856462014TCTTAT10GENIChomozygous128819231
105646201556462015AGA10GENIChomozygous128819232
105646201656462017GC9GENIChomozygous117218772
105646269256462694TA13GENIChomozygous131094500
105646294856462949GA12GENIChomozygous117059718
105646301956463020GA9GENIChomozygous117059720
105646323556463236AG12GENIChomozygous116783576
105646368056463681AG11GENIChomozygous117059722
105646369856463699TC11GENIChomozygous116783578
105646406056464061TC16GENIChomozygous116783580
105646458756464587GAAG22GENIChomozygous131094501
105646477356464774AG23GENICpossibly homozygous116783582
105646624156466242GA15GENIChomozygous117059724
105646642756466428CT20GENIChomozygous117059726
105646651156466512GA17GENIChomozygous116935327
105646739656467397GA18GENIChomozygous116783584
105646779356467794GC22GENIChomozygous116935329
105646939756469397T18GENIChomozygous131094502
105646989356469893AC22GENIChomozygous131094503
105647023056470231AG21GENIChomozygous116935333
105647106856471069AG38GENIChomozygous116935335
105647157856471579TC26GENIChomozygous116783590
105647253756472538TC27GENIChomozygous116935339
105647255256472553AG26GENIChomozygous116783592
105647212356472123C18GENIChomozygous131094504
105647276756472767TATATAG22GENIChomozygous131094505