chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID 1,44313690,44313691,C,T,57,GENIC,heterozygous,924961085 1,44313729,44313730,C,T,35,GENIC,heterozygous,924961086 1,44313939,44313940,T,C,85,GENIC,heterozygous,924961087 1,44313943,44313944,G,A,88,GENIC,heterozygous,924961088 1,44313948,44313949,C,T,94,GENIC,heterozygous,924961089 1,44313952,44313953,G,T,94,GENIC,heterozygous,924961090 1,44313963,44313964,G,T,103,GENIC,heterozygous,924961091 1,44313973,44313974,G,A,101,GENIC,heterozygous,924961092 1,44313977,44313978,C,T,101,GENIC,heterozygous,924961093 1,44313979,44313980,C,T,101,GENIC,heterozygous,924961094 1,44313982,44313983,C,T,99,GENIC,heterozygous,924961095 1,44313984,44313985,C,T,99,GENIC,heterozygous,924961096 1,44314060,44314061,G,C,126,GENIC,heterozygous,924961097 1,44314065,44314066,C,A,122,GENIC,heterozygous,924961098 1,44314071,44314072,T,C,121,GENIC,heterozygous,924961099 1,44314076,44314077,C,T,125,GENIC,heterozygous,924961100 1,44314081,44314082,G,C,122,GENIC,heterozygous,924961101 1,44314083,44314084,C,T,120,GENIC,heterozygous,924961102 1,44314093,44314094,T,C,121,GENIC,heterozygous,924961103 1,44314117,44314118,T,G,114,GENIC,heterozygous,924961104 1,44314124,44314125,A,G,102,GENIC,heterozygous,924961105 1,44314125,44314126,C,T,102,GENIC,heterozygous,924961106 1,44314126,44314127,C,T,106,GENIC,heterozygous,924961107 1,44314153,44314154,C,T,150,GENIC,heterozygous,924961108 1,44314213,44314214,G,A,219,GENIC,heterozygous,924961109 1,44314221,44314222,G,A,211,GENIC,heterozygous,924961110 1,44314228,44314229,A,G,206,GENIC,heterozygous,924961111 1,44314243,44314244,G,C,198,GENIC,heterozygous,924961112