chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 54573720 54573721 G A 33 INTERGENIC possibly homozygous 795495656 13 54573740 54573741 A G 33 INTERGENIC possibly homozygous 795495657 13 54573744 54573745 C T 35 INTERGENIC possibly homozygous 795495658 13 54573765 54573766 T A 40 INTERGENIC homozygous 795495659 13 54573966 54573967 C T 43 INTERGENIC homozygous 795495660 13 54574510 54574511 T C 37 INTERGENIC homozygous 795495661 13 54574761 54574762 G C 44 INTERGENIC homozygous 795495662 13 54575360 54575361 G A 50 INTERGENIC homozygous 795495663 13 54575507 54575508 G A 30 INTERGENIC homozygous 795495664 13 54576396 54576397 T C 54 INTERGENIC homozygous 795495665 13 54576655 54576656 A G 36 INTERGENIC homozygous 795495666 13 54576692 54576693 C T 47 INTERGENIC homozygous 795495667 13 54576937 54576938 A T 31 INTERGENIC possibly homozygous 795495668 13 54577884 54577885 C T 55 INTERGENIC homozygous 795495669 13 54578177 54578178 T C 47 INTERGENIC homozygous 795495670 13 54579101 54579102 A G 38 INTERGENIC homozygous 795495671 13 54579106 54579107 T C 39 INTERGENIC homozygous 795495672 13 54579167 54579168 G A 51 INTERGENIC homozygous 795495673 13 54579563 54579564 A G 33 INTERGENIC homozygous 795495674 13 54579593 54579594 T C 43 INTERGENIC homozygous 795495675 13 54579755 54579756 A G 48 INTERGENIC homozygous 795495676 13 54579869 54579870 A G 27 INTERGENIC possibly homozygous 795495677