chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1099120129912013TC4GENIChomozygous51616110
1099120209912021TC4GENIChomozygous51616111
1099121079912108GA6GENIChomozygous52110797
1099122559912256CCGG1GENIChomozygous52027441
1099124599912460AG10GENIChomozygous52027443
1099131249913125TG26GENIChomozygous52027445
1099131339913134GT25GENIChomozygous52110799
1099132109913211TC16GENIChomozygous51616113
1099133449913345AG20GENIChomozygous51616114
1099136979913698GT20GENIChomozygous51616115
1099136999913700GA19GENIChomozygous52027451
1099138249913825AC21GENIChomozygous51616116
1099141189914119CT18GENIChomozygous52027455
1099141409914141G-21GENIChomozygous52027457
1099141919914192AG20GENIChomozygous51616117
1099142209914221GT9GENIChomozygous52027459
1099144759914476AG26GENIChomozygous51616118
1099152549915255TTC14GENIChomozygous51616121
1099163029916303A-16GENIChomozygous52027461
1099164289916437AGAGCAGTC---------9GENIChomozygous52027463
1099164509916451TA13GENIChomozygous51616124
1099177599917760AG25GENIChomozygous51616126
1099183239918324AG19GENIChomozygous51323669
1099136679913668CA24GENIChomozygous51323666
1099165929916593TTC14GENIChomozygous51323667
1099188409918841CT21GENIChomozygous52027465
1099188499918850TC20GENIChomozygous52027467
1099189969918997TC15GENIChomozygous52027469
1099191649919165TC20GENIChomozygous52027471