chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
194248068142480682TC15GENIChomozygous640005388
194248075442480755TA13GENIChomozygous640005389
194248099642480997GT8GENIChomozygous640005390
194248274642482747AATGTG7GENICpossibly homozygous751019740
194248315242483153GA13GENIChomozygous640005391
194248342542483426GT11GENIChomozygous640005392
194248496642484967CT9GENIChomozygous640005393
194248497442484975TC9GENIChomozygous640005394
194248497842484985TCTCTCT-------10GENIChomozygous751019742
194248498842484989TC4GENIChomozygous640005395
194248499042484991TC4GENIChomozygous640005396
194248499242484993TC6GENIChomozygous640005397
194248530242485303T-16GENICpossibly homozygous751019743
194248535942485360TC13GENIChomozygous640005398
194248585642485859AAA---11GENICheterozygous751019745
194248585742485859AA--11GENICheterozygous751019746
194248597342485974TG22GENIChomozygous640005399
194248619042486191AG23GENIChomozygous640005400
194248760842487609TC8GENIChomozygous640005401
194248779742487798TC26GENIChomozygous640005402
194248859842488599AG34GENIChomozygous640005403
194248891742488918CT19GENIChomozygous640005404
194248903242489033AG17GENIChomozygous640005405
194248976142489837GAGCCATGCTTTTCTTTTTTTTTTTTTTTTCTTTTGGTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTG----------------------------------------------------------------------------13GENIChomozygous751019747
194249011442490115CG29GENIChomozygous640005406
194249064542490646TTGTTCG26GENIChomozygous751019748