chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101391406613914067CT61GENIChomozygous116736542
101391414613914147T50GENICpossibly homozygous131087879
101391445413914455TC59GENIChomozygous116736543
101391451613914517TG53GENIChomozygous116736544
101391740113917402GA55GENIChomozygous116736545
101391969613919704TTTTCTTT40GENIChomozygous131087880
101391970713919707T40GENIChomozygous131087881
101391992013919921G38GENIChomozygous131087882
101391993013919931CT39GENIChomozygous116736546
101392009513920095G45GENIChomozygous131087883
101392013113920132CA38GENICpossibly homozygous116736547
101392037413920374A54GENIChomozygous131087884
101392113113921131T42GENIChomozygous131087885
101392181613921817TC51GENIChomozygous116736548
101392243613922437GA49GENIChomozygous116736549
101392390413923905TC61GENIChomozygous116736550
101392619913926200AT48GENIChomozygous116736551
101392635613926357CT57GENIChomozygous116736552
101392806813928068TTTTTTTG40GENICpossibly homozygous131087886
101393100913931010TC59GENICpossibly homozygous116736553
101393478313934784AG50GENIChomozygous116736554
101393538913935390AG48GENIChomozygous116736555
101393557213935573GA59GENIChomozygous116736556
101393886913938870TC46GENIChomozygous116736557
101394116013941161AG53GENIChomozygous116736558
101394789013947891AG50GENIChomozygous116736559
101394800013948001TC61GENIChomozygous116736560
101394800713948008AC60GENIChomozygous116736561
101395142613951427AG34GENIChomozygous116736563
101395699613956997TC55GENIChomozygous116736564
101395786913957870GC48GENIChomozygous116736565
101391972113919722TC40GENIChomozygous118030560
101392147913921601GGGCCTAGAATTTCTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTCGGAGCTGGGGATCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCCAA21GENICpossibly homozygous131463482