chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159976211499762115CT21GENIChomozygous112760485
159976219799762198CG29GENIChomozygous112616605
159976220899762209AG30GENIChomozygous112616606
159976245699762457CT30GENIChomozygous112760487
159976262399762624CA36GENIChomozygous112760489
159976283899762839TA29GENIChomozygous112616607
159976345099763451AG20GENIChomozygous112616610
159976351899763519GA23GENIChomozygous112760491
159976364099763641AG30GENIChomozygous112616611
159976434499764345CA34GENIChomozygous112760493
159976467799764678TA17GENIChomozygous112760495
159976506999765070CT21GENIChomozygous112760497
159976536599765366TC22GENIChomozygous112616637
159976644599766446CT31GENIChomozygous112760499
159976754499767545GT26GENIChomozygous112760501
159976801999768020TA27GENIChomozygous112760505
159976988399769884CT33GENIChomozygous112760509
159977078299770783TC15GENIChomozygous112760517
159977099099770991TG21GENIChomozygous112760519
159977103499771035AC15GENIChomozygous112760521
159977132399771324AG16GENIChomozygous112616661