chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 10054372 10054373 A C 23 INTERGENIC homozygous 795618353 14 10057999 10058000 T C 40 INTERGENIC homozygous 795618354 14 10058158 10058159 T A 21 INTERGENIC heterozygous 795618355 14 10058372 10058373 A G 30 INTERGENIC possibly homozygous 795618356 14 10058393 10058394 A C 31 INTERGENIC possibly homozygous 795618357 14 10058545 10058546 C A 39 INTERGENIC homozygous 795618358 14 10058896 10058897 G A 41 INTERGENIC homozygous 795618359 14 10060770 10060771 C T 45 GENIC homozygous 795618360 14 10060820 10060821 A G 45 GENIC homozygous 795618361 14 10060966 10060967 C T 52 GENIC possibly homozygous 795618362 14 10061087 10061088 G C 48 GENIC homozygous 795618363 14 10061140 10061141 C T 42 GENIC homozygous 795618364 14 10061142 10061143 A T 40 GENIC homozygous 795618365 14 10061153 10061154 T C 42 GENIC homozygous 795618366 14 10061198 10061199 G A 44 GENIC homozygous 795618367 14 10061294 10061295 G T 22 GENIC homozygous 795618368 14 10061302 10061303 G T 28 GENIC heterozygous 795618369 14 10061314 10061315 A G 28 GENIC heterozygous 795618370 14 10061414 10061415 A C 33 GENIC homozygous 795618371 14 10061420 10061421 G A 35 GENIC homozygous 795618372 14 10061423 10061424 T A 36 GENIC homozygous 795618373 14 10061446 10061447 C A 30 GENIC homozygous 795618374 14 10061579 10061580 A G 38 GENIC homozygous 795618375 14 10061585 10061586 A G 38 GENIC homozygous 795618376 14 10061595 10061596 G A 39 GENIC homozygous 795618377 14 10061631 10061632 C T 40 GENIC homozygous 795618378 14 10061686 10061687 T C 50 GENIC homozygous 795618379 14 10061693 10061694 A G 44 GENIC homozygous 795618380 14 10061694 10061695 A G 45 GENIC homozygous 795618381 14 10061700 10061701 C T 49 GENIC homozygous 795618382 14 10061873 10061874 G A 28 GENIC homozygous 795618383 14 10061875 10061876 C A 30 GENIC homozygous 795618384