chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 37564004 37564005 C A 26 GENIC homozygous 955981913 12 37564549 37564550 T C 43 GENIC homozygous 955981914 12 37564784 37564785 T C 38 GENIC homozygous 955981915 12 37566834 37566835 A G 6 GENIC homozygous 955981916 12 37567045 37567046 T C 36 GENIC homozygous 955981917 12 37567397 37567398 T C 44 GENIC homozygous 955981918 12 37567898 37567899 C T 18 GENIC homozygous 955981919 12 37567939 37567940 A C 20 GENIC homozygous 955981920 12 37569481 37569482 C G 23 GENIC homozygous 955981921 12 37569732 37569733 G A 23 GENIC homozygous 955981922 12 37570869 37570870 G A 37 GENIC homozygous 955981923 12 37571673 37571674 A G 26 GENIC homozygous 955981924 12 37572327 37572328 G A 41 GENIC homozygous 955981925 12 37574609 37574610 C A 14 GENIC homozygous 955981926 12 37574610 37574611 T G 14 GENIC homozygous 955981927 12 37574619 37574620 A G 11 GENIC homozygous 955981928 12 37574633 37574634 C G 9 GENIC homozygous 955981929 12 37578715 37578716 C A 27 GENIC homozygous 955981930 12 37579482 37579483 T C 30 GENIC homozygous 955981931 12 37579958 37579959 C T 46 GENIC homozygous 955981932