chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 30880472 30880473 T C 16 GENIC homozygous 941846804 11 30880650 30880651 A G 29 GENIC homozygous 941846805 11 30881286 30881287 T C 39 GENIC homozygous 941846806 11 30882026 30882027 G A 30 GENIC homozygous 941846807 11 30883071 30883072 A G 11 GENIC homozygous 941846808 11 30883155 30883156 T A 12 GENIC homozygous 941846809 11 30883216 30883217 T C 19 GENIC homozygous 941846810 11 30884111 30884112 A G 21 GENIC homozygous 941846811 11 30884206 30884207 T C 22 GENIC homozygous 941846812 11 30884486 30884487 A G 23 GENIC homozygous 941846813 11 30886612 30886613 G C 23 GENIC homozygous 941846814 11 30886629 30886630 A G 21 GENIC homozygous 941846815 11 30886858 30886859 A G 19 GENIC homozygous 941846816 11 30887179 30887180 T C 36 GENIC homozygous 941846817 11 30887639 30887640 T C 19 GENIC homozygous 941846818 11 30889474 30889475 T C 37 GENIC homozygous 941846819 11 30889480 30889481 A G 36 GENIC homozygous 941846820 11 30890808 30890809 A G 22 GENIC homozygous 941846821 11 30890862 30890863 G A 26 GENIC homozygous 941846822 11 30891923 30891924 T A 11 GENIC homozygous 941846823 11 30893243 30893244 G T 30 GENIC homozygous 941846824