chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101139718211397182C32GENIChomozygous128789877
101140526011405261GT17GENICpossibly homozygous118026676
101140525611405257GA18GENICpossibly homozygous118092870
101140529411405295GT5GENICheterozygous130395837
101143333611433336GG33GENIChomozygous128789893
101144780311447804GC8GENIChomozygous130395838
101144780511447806TC8GENIChomozygous130395839
101144782411447825TC12GENIChomozygous130395840
101144784111447842GC15GENIChomozygous128865357
101145416511454165G40GENIChomozygous128789902
101144784111447841C16GENIChomozygous128789900
101144784411447845GA16GENIChomozygous128865358
101145418811454188G40GENIChomozygous128789903
101145468311454684T13GENIChomozygous131901113
101145419411454195T37GENIChomozygous128789904
101145420011454200G34GENIChomozygous128789905
101145424911454249A40GENIChomozygous128789906
101145467411454674T16GENIChomozygous131901112
101145464611454647A20GENIChomozygous133423789
101145465411454654C18GENIChomozygous133423790
101145422111454222TG38GENICpossibly homozygous116494743
101145469311454693A11GENIChomozygous131901114
101145469911454700G10GENIChomozygous131901115
101145471311454714T8GENIChomozygous131901116
101145566211455663TA52GENIChomozygous116494749
101145566311455664TC52GENIChomozygous116494751
101145566411455665TC53GENIChomozygous116494753
101145613211456132CCA50GENIChomozygous128789907
101145740811457448CAGTATGCTCTCATGTCCCCATTGTCCAGTGGTGTCCTTT39GENIChomozygous128789908
101148064511480646C35GENIChomozygous128789921
101148065011480651C35GENIChomozygous128789922
101148066511480666CT36GENIChomozygous117981396
101148070511480706A34GENIChomozygous128789923
101148071011480711C38GENIChomozygous128789924