chr start stop reference nuc variant nuc depth genic status zygosity variant ID 13 54573720 54573721 G A 17 INTERGENIC homozygous 804464491 13 54573740 54573741 A G 13 INTERGENIC homozygous 804464492 13 54573744 54573745 C T 13 INTERGENIC homozygous 804464493 13 54573765 54573766 T A 16 INTERGENIC homozygous 804464494 13 54573966 54573967 C T 12 INTERGENIC homozygous 804464495 13 54574510 54574511 T C 8 INTERGENIC homozygous 804464496 13 54574761 54574762 G C 21 INTERGENIC homozygous 804464497 13 54575360 54575361 G A 13 INTERGENIC homozygous 804464498 13 54575507 54575508 G A 9 INTERGENIC homozygous 804464499 13 54576396 54576397 T C 20 INTERGENIC homozygous 804464500 13 54576655 54576656 A G 21 INTERGENIC homozygous 804464501 13 54576692 54576693 C T 31 INTERGENIC homozygous 804464502 13 54576937 54576938 A T 21 INTERGENIC homozygous 804464503 13 54577884 54577885 C T 6 INTERGENIC homozygous 804464504 13 54578177 54578178 T C 11 INTERGENIC homozygous 804464505 13 54579101 54579102 A G 13 INTERGENIC homozygous 804464506 13 54579106 54579107 T C 13 INTERGENIC possibly homozygous 804464507 13 54579167 54579168 G A 11 INTERGENIC homozygous 804464508 13 54579563 54579564 A G 11 INTERGENIC possibly homozygous 804464509 13 54579593 54579594 T C 8 INTERGENIC homozygous 804464510 13 54579755 54579756 A G 20 INTERGENIC homozygous 804464511 13 54579869 54579870 A G 19 INTERGENIC homozygous 804464512