chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 40247747 40247748 G C 21 GENIC homozygous 804026993 10 40248280 40248281 C G 28 GENIC homozygous 804026994 10 40248287 40248288 A G 28 GENIC homozygous 804026995 10 40248300 40248301 C T 26 GENIC homozygous 804026996 10 40248480 40248481 C A 21 GENIC homozygous 804026997 10 40248587 40248588 C G 26 GENIC homozygous 804026998 10 40248638 40248639 C T 32 GENIC homozygous 804026999 10 40248938 40248939 T C 28 GENIC homozygous 804027000 10 40249115 40249116 C G 46 GENIC homozygous 804027001 10 40249700 40249701 T C 19 GENIC homozygous 804027002 10 40249947 40249948 T G 28 GENIC homozygous 804027003 10 40251240 40251241 G A 8 GENIC homozygous 804027004 10 40251529 40251530 T C 21 GENIC homozygous 804027005 10 40251735 40251736 A G 24 GENIC homozygous 804027006 10 40252051 40252052 C T 22 GENIC homozygous 804027007 10 40252066 40252067 T C 20 GENIC homozygous 804027008 10 40252934 40252935 T C 22 GENIC homozygous 804027009 10 40253038 40253039 T C 35 GENIC possibly homozygous 804027010 10 40253450 40253451 C T 35 GENIC homozygous 804027011 10 40253751 40253752 T C 29 GENIC homozygous 804027012 10 40253991 40253992 T C 26 GENIC homozygous 804027013 10 40254191 40254192 A C 36 GENIC homozygous 804027014 10 40254347 40254348 A G 20 GENIC homozygous 804027015 10 40254376 40254377 G A 19 GENIC homozygous 804027016 10 40254433 40254434 A G 21 GENIC homozygous 804027017 10 40254710 40254711 T C 23 GENIC homozygous 804027018 10 40254874 40254875 C T 13 GENIC homozygous 804027019 10 40254993 40254994 G A 22 GENIC homozygous 804027020