chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 37559858 37559859 C T 11 GENIC heterozygous 874790979 12 37564004 37564005 C A 13 GENIC homozygous 874790980 12 37564549 37564550 T C 8 GENIC homozygous 874790981 12 37564784 37564785 T C 21 GENIC homozygous 874790982 12 37566834 37566835 A G 8 GENIC homozygous 874790983 12 37567397 37567398 T C 12 GENIC homozygous 874790984 12 37567898 37567899 C T 17 GENIC homozygous 874790985 12 37567939 37567940 A C 15 GENIC homozygous 874790986 12 37569481 37569482 C G 16 GENIC homozygous 874790987 12 37569732 37569733 G A 24 GENIC homozygous 874790988 12 37570869 37570870 G A 6 GENIC homozygous 874790989 12 37571673 37571674 A G 14 GENIC homozygous 874790990 12 37572327 37572328 G A 29 GENIC homozygous 874790991 12 37576292 37576293 G A 21 GENIC homozygous 874790992 12 37578381 37578382 T C 27 GENIC homozygous 874790993 12 37578715 37578716 C A 26 GENIC homozygous 874790994 12 37579958 37579959 C T 8 GENIC homozygous 874790995