chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 54573720 54573721 G A 17 GENIC homozygous 973629105 13 54573740 54573741 A G 14 GENIC homozygous 973629106 13 54573744 54573745 C T 14 GENIC homozygous 973629107 13 54574510 54574511 T C 8 GENIC homozygous 973629108 13 54574761 54574762 G C 16 GENIC homozygous 973629109 13 54575360 54575361 G A 11 GENIC homozygous 973629110 13 54575507 54575508 G A 9 GENIC homozygous 973629111 13 54576396 54576397 T C 21 GENIC homozygous 973629112 13 54576655 54576656 A G 21 GENIC homozygous 973629113 13 54576692 54576693 C T 30 GENIC homozygous 973629114 13 54576937 54576938 A T 20 GENIC homozygous 973629115 13 54577884 54577885 C T 6 GENIC homozygous 973629116 13 54578177 54578178 T C 12 GENIC homozygous 973629117 13 54579101 54579102 A G 12 GENIC homozygous 973629118 13 54579106 54579107 T C 12 GENIC possibly homozygous 973629119 13 54579167 54579168 G A 12 GENIC homozygous 973629120 13 54579563 54579564 A G 9 GENIC homozygous 973629121 13 54579593 54579594 T C 8 GENIC homozygous 973629122 13 54579755 54579756 A G 18 GENIC homozygous 973629123 13 54579869 54579870 A G 13 GENIC homozygous 973629124