chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 30880650 30880651 A G 29 GENIC homozygous 929954676 11 30881150 30881151 C T 51 GENIC homozygous 929954677 11 30881388 30881389 T C 24 GENIC homozygous 929954678 11 30883216 30883217 T C 33 GENIC homozygous 929954679 11 30884486 30884487 A G 28 GENIC homozygous 929954680 11 30885831 30885832 C T 45 GENIC homozygous 929954681 11 30886157 30886158 C T 34 GENIC homozygous 929954682 11 30886629 30886630 A G 37 GENIC homozygous 929954683 11 30887179 30887180 T C 49 GENIC homozygous 929954684 11 30887257 30887258 G A 45 GENIC homozygous 929954685 11 30889480 30889481 A G 39 GENIC homozygous 929954686 11 30889600 30889601 C T 51 GENIC homozygous 929954687 11 30889921 30889922 T G 37 GENIC homozygous 929954688 11 30890081 30890082 T G 26 GENIC homozygous 929954689 11 30892838 30892839 T C 24 GENIC homozygous 929954690