chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109727034109727035TC20GENIChomozygous68253674
10109728155109728156AG4GENIChomozygous68253683
10109731018109731019GA16GENIChomozygous68253687
10109731350109731350AAT17GENICheterozygous69289248
10109731844109731845AG19GENIChomozygous68253690
10109732254109732255CT7GENIChomozygous68253694
10109732956109732957AC13GENIChomozygous68253697
10109733366109733367GA8GENIChomozygous68253700
10109733618109733619AG14GENIChomozygous68253704
10109733750109733751AG8GENIChomozygous68253707
10109733815109733816GT8GENIChomozygous68253710