chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 90216401 90216402 T C 37 GENIC possibly homozygous 116108708 11 90216492 90216493 G A 24 GENIC homozygous 116108709 11 90216861 90216862 A G 30 GENIC homozygous 116108710 11 90217235 90217236 A G 25 GENIC homozygous 116108711 11 90218408 90218409 C T 26 GENIC homozygous 116108712 11 90220093 90220094 C T 29 GENIC homozygous 116108714 11 90220822 90220823 A G 31 GENIC homozygous 115933691 11 90220852 90220853 T A 36 GENIC homozygous 115933693 11 90220875 90220876 A G 36 GENIC homozygous 115933695 11 90223275 90223276 G A 30 GENIC homozygous 116108715 11 90223640 90223641 G A 28 GENIC homozygous 116108716 11 90223783 90223784 G A 19 GENIC homozygous 116108717 11 90225017 90225018 C T 31 GENIC possibly homozygous 116108718 11 90225314 90225315 A G 22 GENIC homozygous 116108719 11 90225731 90225732 C T 30 GENIC possibly homozygous 116108720 11 90226514 90226515 T A 4 GENIC homozygous 116108722 11 90229089 90229090 C A 33 GENIC possibly homozygous 116108723 11 90229339 90229340 G A 41 GENIC homozygous 116108724 11 90229376 90229377 G A 35 GENIC homozygous 116108725 11 90229515 90229516 G A 24 GENIC homozygous 116108726 11 90230592 90230593 A C 19 GENIC homozygous 116108727 11 90231108 90231109 C T 22 GENIC homozygous 116299414 11 90234286 90234287 C A 13 GENIC homozygous 115933697