chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103921414339214144CT58GENICheterozygous128867915
103921415539214156A58GENICheterozygous128808753
103921430539214306GC73GENICheterozygous118065799
103921431839214319TC70GENICheterozygous118065800
103921441539214416TC58GENICheterozygous117989751
103921443039214431TC65GENICheterozygous117989752
103921447039214471TA88GENICheterozygous130396600
103921449839214499TC103GENICheterozygous117989753
103921459839214599TC93GENICheterozygous117989754
103921460439214605CT92GENICheterozygous117989755
103921471939214720G69GENICheterozygous128808754
103921472139214722AT68GENICheterozygous123344053
103921481739214818T92GENICheterozygous128808755
103921482739214828AC94GENICheterozygous117277730
103921488539214886TC96GENICheterozygous116566513
103921490039214901GC105GENICheterozygous117277732
103921512139215122AT55GENICheterozygous123344056
103921512239215123GA57GENICheterozygous123344057
103921515639215159CTT61GENICheterozygous128808756
103921526139215262TC68GENICheterozygous116763000
103921526739215268AG67GENICheterozygous116763002
103921530339215304AG66GENICheterozygous117217674
103921531339215315TC58GENICheterozygous128808757
103921532239215324TG60GENICheterozygous128808758
103921532739215327AC61GENICheterozygous128808759
103921729939217299ACACTCTGGTTT56GENICheterozygous128808760