chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171049571710495717G11GENIChomozygous129421538
171051586010515860A40GENIChomozygous129421551
171051586510515866A42GENIChomozygous129421552
171051594810515949T46GENIChomozygous129421553
171051596010515960A48GENIChomozygous129421554
171051597110515971A45GENIChomozygous129421555
171051598910515989A44GENIChomozygous129421556
171051600610516006A42GENIChomozygous129421557
171051601310516013T42GENIChomozygous129421558
171051602510516025A42GENIChomozygous129421559
171051603410516034ATTT37GENIChomozygous129421560
171051604910516050A36GENIChomozygous129421561
171051605410516055G37GENIChomozygous129421562
171051609710516098CA35GENIChomozygous119263977
171051609910516099A35GENIChomozygous129421563
171051615410516154C36GENIChomozygous129421564
171051617110516174CGC33GENIChomozygous129421565
171051617710516178GT33GENIChomozygous124297690
171051620010516201C36GENIChomozygous129421566
171051620810516209A36GENIChomozygous129421567
171051622510516225A39GENIChomozygous129421568
171051623210516232A36GENIChomozygous129421569
171051623410516234T38GENIChomozygous129421570
171051626810516269TC39GENIChomozygous110954306
171051627810516279T40GENIChomozygous129421571
171051628510516286G43GENIChomozygous129421572
171052768510527685C38GENIChomozygous129421581
171050997910509981GT16GENICheterozygous130461540
171052130710521308A10GENICheterozygous130461541