chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 75059058 75059059 A G 34 GENIC homozygous 813190236 10 75059257 75059258 C T 26 GENIC homozygous 813190237 10 75067597 75067598 T C 9 GENIC homozygous 813190238 10 75072157 75072158 A G 23 GENIC homozygous 813190239 10 75073541 75073542 A G 24 GENIC homozygous 813190240 10 75073706 75073707 T C 25 GENIC homozygous 813190241 10 75073727 75073728 T C 27 GENIC homozygous 813190242 10 75073858 75073859 T C 25 GENIC homozygous 813190243 10 75074282 75074283 G A 43 GENIC possibly homozygous 813190244 10 75075386 75075387 T C 46 GENIC homozygous 813190245 10 75075487 75075488 A G 38 GENIC homozygous 813190246 10 75075644 75075645 G A 32 GENIC homozygous 813190247 10 75075825 75075826 C G 34 GENIC homozygous 813190248 10 75075911 75075912 T C 31 GENIC homozygous 813190249 10 75076145 75076146 A T 29 GENIC homozygous 813190250 10 75076498 75076499 C T 36 GENIC homozygous 813190251 10 75076934 75076935 A G 30 GENIC possibly homozygous 813190252 10 75077054 75077055 A G 41 GENIC homozygous 813190253 10 75077622 75077623 C T 36 GENIC homozygous 813190254 10 75078367 75078368 G A 68 GENIC homozygous 813190255 10 75078806 75078807 T C 39 INTERGENIC homozygous 813190256