chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 10058372 10058373 A G 36 GENIC homozygous 930224288 14 10058393 10058394 A C 36 GENIC homozygous 930224289 14 10058545 10058546 C A 35 GENIC homozygous 930224290 14 10058589 10058590 C T 37 GENIC homozygous 930224291 14 10058695 10058696 C T 34 GENIC homozygous 930224292 14 10058896 10058897 G A 43 GENIC homozygous 930224293 14 10059349 10059350 G A 32 GENIC homozygous 930224294 14 10060743 10060744 C T 27 GENIC homozygous 930224295 14 10060820 10060821 A G 40 GENIC homozygous 930224296 14 10060966 10060967 C T 30 GENIC homozygous 930224297 14 10061087 10061088 G C 57 GENIC homozygous 930224298 14 10061140 10061141 C T 53 GENIC homozygous 930224299 14 10061142 10061143 A T 53 GENIC homozygous 930224300 14 10061153 10061154 T C 51 GENIC homozygous 930224301 14 10061198 10061199 G A 42 GENIC homozygous 930224302 14 10061414 10061415 A C 33 GENIC possibly homozygous 930224303 14 10061420 10061421 G A 36 GENIC homozygous 930224304 14 10061423 10061424 T A 37 GENIC homozygous 930224305 14 10061446 10061447 C A 41 GENIC homozygous 930224306 14 10061579 10061580 A G 45 GENIC homozygous 930224307 14 10061585 10061586 A G 38 GENIC homozygous 930224308 14 10061595 10061596 G A 45 GENIC homozygous 930224309 14 10061631 10061632 C T 43 GENIC homozygous 930224310 14 10061686 10061687 T C 39 GENIC homozygous 930224311 14 10061693 10061694 A G 38 GENIC homozygous 930224312 14 10061694 10061695 A G 40 GENIC homozygous 930224313 14 10061700 10061701 C T 41 GENIC homozygous 930224314 14 10061873 10061874 G A 44 GENIC homozygous 930224315 14 10061875 10061876 C A 45 GENIC homozygous 930224316