chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 37564004 37564005 C A 23 GENIC homozygous 983165991 12 37564549 37564550 T C 27 GENIC homozygous 983165992 12 37564784 37564785 T C 9 GENIC homozygous 983165993 12 37566834 37566835 A G 9 GENIC homozygous 983165994 12 37567045 37567046 T C 16 GENIC homozygous 983165995 12 37567397 37567398 T C 16 GENIC homozygous 983165996 12 37567898 37567899 C T 23 GENIC homozygous 983165997 12 37567939 37567940 A C 31 GENIC homozygous 983165998 12 37569481 37569482 C G 14 GENIC homozygous 983165999 12 37569732 37569733 G A 18 GENIC homozygous 983166000 12 37570869 37570870 G A 17 GENIC homozygous 983166001 12 37571673 37571674 A G 22 GENIC homozygous 983166002 12 37572327 37572328 G A 23 GENIC homozygous 983166003 12 37576292 37576293 G A 21 GENIC homozygous 983166004 12 37578715 37578716 C A 34 GENIC homozygous 983166005 12 37579482 37579483 T C 11 GENIC homozygous 983166006 12 37579916 37579917 G T 9 GENIC homozygous 983166007 12 37579917 37579918 A G 10 GENIC homozygous 983166008 12 37579958 37579959 C T 9 GENIC homozygous 983166009