chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 264094261 264094262 T C 28 GENIC possibly homozygous 992765721 1 264095002 264095003 T C 31 GENIC possibly homozygous 992765722 1 264095472 264095473 T C 33 GENIC homozygous 992765723 1 264095886 264095887 A G 29 GENIC possibly homozygous 992765724 1 264096218 264096219 C T 36 GENIC possibly homozygous 992765725 1 264096731 264096732 G A 32 GENIC homozygous 992765726 1 264097115 264097116 C T 24 GENIC homozygous 992765727 1 264097200 264097201 G A 35 GENIC possibly homozygous 992765728 1 264097208 264097209 T C 35 GENIC possibly homozygous 992765729 1 264097432 264097433 T C 19 GENIC homozygous 992765730 1 264097633 264097634 A C 39 GENIC homozygous 992765731 1 264098036 264098037 G T 26 GENIC possibly homozygous 992765732 1 264098042 264098043 G A 25 GENIC possibly homozygous 992765733 1 264098403 264098404 T C 20 GENIC homozygous 992765734 1 264098424 264098425 G A 23 GENIC homozygous 992765735 1 264099176 264099177 G A 18 GENIC possibly homozygous 992765736 1 264099576 264099577 C T 11 GENIC possibly homozygous 992765737 1 264099875 264099876 C T 35 GENIC possibly homozygous 992765738 1 264100059 264100060 T A 27 GENIC homozygous 992765739 1 264100188 264100189 A G 23 GENIC homozygous 992765740 1 264100212 264100213 T G 20 GENIC possibly homozygous 992765741 1 264100452 264100453 C A 25 GENIC possibly homozygous 992765742 1 264100637 264100638 T C 36 GENIC homozygous 992765743 1 264100695 264100696 G A 35 GENIC possibly homozygous 992765744 1 264101486 264101487 C G 5 GENIC homozygous 992765745 1 264103421 264103422 C T 30 GENIC homozygous 992765746 1 264105400 264105401 T G 35 GENIC possibly homozygous 992765747 1 264105443 264105444 A C 26 GENIC homozygous 992765748