chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 146073852 146073853 G A 24 GENIC homozygous 113393224 4 146075143 146075144 A G 33 GENIC homozygous 112871849 4 146075607 146075608 T C 34 GENIC possibly homozygous 113393226 4 146076145 146076146 A G 40 GENIC homozygous 112871852 4 146077033 146077034 C T 43 GENIC homozygous 113393228 4 146077138 146077139 A G 30 GENIC homozygous 112871853 4 146077769 146077770 A G 41 GENIC homozygous 112871856 4 146077979 146077980 T C 20 GENIC homozygous 112871857 4 146079618 146079619 T C 35 GENIC homozygous 112871858 4 146079948 146079949 G A 39 GENIC homozygous 113393230 4 146080107 146080108 G T 34 GENIC homozygous 113393232 4 146084144 146084145 C T 25 GENIC homozygous 112871885 4 146084440 146084441 T C 29 GENIC homozygous 112871886 4 146084596 146084597 G A 35 GENIC homozygous 112871887 4 146084656 146084657 C A 28 GENIC homozygous 112871888 4 146085071 146085072 A C 45 GENIC homozygous 112871889 4 146085380 146085381 C T 45 GENIC homozygous 112871891 4 146085479 146085480 C T 39 GENIC homozygous 112871892 4 146085517 146085518 T C 28 GENIC homozygous 112871893 4 146085552 146085553 G T 25 GENIC homozygous 112871894 4 146085763 146085764 G C 25 GENIC homozygous 112871895