chr,start,stop,reference nuc,variant nuc,depth,genic status,zygosity,variant ID X,71476949,71476951,TC,--,3,GENIC,heterozygous,45569736 X,71477583,71477584,G,-,8,GENIC,heterozygous,45547644 X,71481482,71481483,A,-,5,GENIC,heterozygous,45511865 X,71487350,71487351,C,CAG,2,GENIC,heterozygous,45569738 X,71507311,71507312,C,CTTACTTTTGGCTGCTACTGTGTGTCTAGAAGCTTGGAGGAGATGGGCTTTGTGGAAGAAT,10,GENIC,homozygous,45511867 X,71507315,71507316,C,CCTAATGCTCCTTGGGG,8,GENIC,homozygous,45511869 X,71519150,71519151,A,AG,8,GENIC,homozygous,45146798