chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 33174616 33174617 A G 14 GENIC homozygous 975617051 5 33176371 33176372 G A 6 GENIC homozygous 975617052 5 33177051 33177052 A C 10 GENIC homozygous 975617053 5 33177542 33177543 G A 9 GENIC heterozygous 975617054 5 33177642 33177643 G A 18 GENIC heterozygous 975617055 5 33177668 33177669 C A 17 GENIC heterozygous 975617056 5 33177751 33177752 G T 28 GENIC heterozygous 975617057 5 33177994 33177995 G A 10 GENIC heterozygous 975617058 5 33178007 33178008 G A 11 GENIC heterozygous 975617059 5 33178080 33178081 G A 17 GENIC heterozygous 975617060 5 33178159 33178160 C T 19 GENIC heterozygous 975617061 5 33178210 33178211 C G 19 GENIC heterozygous 975617062 5 33178216 33178217 G A 17 GENIC heterozygous 975617063 5 33178221 33178222 A G 18 GENIC heterozygous 975617064 5 33178226 33178227 A G 20 GENIC heterozygous 975617065 5 33178231 33178232 G T 20 GENIC heterozygous 975617066 5 33179644 33179645 A G 12 GENIC homozygous 975617067 5 33180442 33180443 C T 9 GENIC homozygous 975617068 5 33180660 33180661 T C 10 GENIC homozygous 975617069 5 33180995 33180996 G A 4 GENIC homozygous 975617070