chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 31836137 31836138 G A 26 GENIC homozygous 783437032 1 31836401 31836402 T G 12 GENIC heterozygous 783437033 1 31837026 31837027 G A 23 GENIC homozygous 783437034 1 31839379 31839380 A C 21 GENIC possibly homozygous 783437035 1 31840006 31840007 C A 33 GENIC homozygous 783437036 1 31844867 31844868 G A 41 GENIC heterozygous 783437037 1 31846570 31846571 C T 25 GENIC possibly homozygous 783437038 1 31851939 31851940 C T 22 GENIC homozygous 783437039 1 31857503 31857504 A G 27 GENIC homozygous 783437040 1 31858210 31858211 A T 24 GENIC homozygous 783437041 1 31860076 31860077 G A 26 GENIC homozygous 783437042 1 31861499 31861500 T C 30 GENIC homozygous 783437043 1 31861979 31861980 G A 28 GENIC homozygous 783437044 1 31863407 31863408 T C 27 GENIC homozygous 783437045 1 31863414 31863415 T G 31 GENIC homozygous 783437046 1 31864850 31864851 C T 15 GENIC homozygous 783437047