chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3153569683153569684CG57GENIChomozygous136843599
3153569702153569726GGCAGACGAATTCTAACGACCCCT57GENIChomozygous136596610
3153570131153570132GA49GENIChomozygous136843600
3153570269153570270AG31GENIChomozygous136843601
3153570574153570575TC51GENIChomozygous136843602
3153570815153570816CT42GENIChomozygous136843603
3153570816153570817GA42GENIChomozygous136843604
3153571600153571600T46GENIChomozygous136596611
3153572307153572308GC49GENIChomozygous136843605
3153572486153572487CT48GENICpossibly homozygous136843606
3153572552153572553AG57GENICpossibly homozygous136843607
3153573067153573068AG52GENIChomozygous136843608
3153573158153573159GA52GENIChomozygous136843609
3153573182153573183GA51GENIChomozygous136843610
3153573253153573254GT44GENIChomozygous136843611
3153573555153573556GT51GENICpossibly homozygous136843612
3153573761153573762TA54GENIChomozygous136843613
3153573884153573885AG59GENIChomozygous136843614
3153574244153574245GC53GENIChomozygous136843615
3153574251153574252TC53GENIChomozygous136843616
3153574319153574320TC55GENIChomozygous136843617
3153574340153574341TC54GENIChomozygous136843618
3153574365153574367CT61GENIChomozygous136596612
3153574695153574696CG43GENIChomozygous136843619
3153574853153574854TC54GENIChomozygous136843620