chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 33176139 33176140 C T 16 GENIC homozygous 969572733 5 33177051 33177052 A C 20 GENIC homozygous 969572734 5 33177272 33177273 C T 35 GENIC heterozygous 969572735 5 33177585 33177586 T C 26 GENIC heterozygous 969572736 5 33177642 33177643 G A 27 GENIC heterozygous 969572737 5 33177668 33177669 C A 29 GENIC heterozygous 969572738 5 33177751 33177752 G T 41 GENIC heterozygous 969572739 5 33177776 33177777 T C 40 GENIC heterozygous 969572740 5 33177853 33177854 A G 34 GENIC heterozygous 969572741 5 33177994 33177995 G A 26 GENIC heterozygous 969572742 5 33178007 33178008 G A 26 GENIC heterozygous 969572743 5 33178076 33178077 C A 34 GENIC heterozygous 969572744 5 33178080 33178081 G A 35 GENIC heterozygous 969572745 5 33178083 33178084 G A 33 GENIC heterozygous 969572746 5 33178112 33178113 G A 39 GENIC heterozygous 969572747 5 33178159 33178160 C T 30 GENIC heterozygous 969572748 5 33178210 33178211 C G 16 GENIC heterozygous 969572749 5 33178216 33178217 G A 13 GENIC heterozygous 969572750 5 33178678 33178679 G C 31 GENIC heterozygous 969572751 5 33178679 33178680 G T 33 GENIC heterozygous 969572752 5 33179644 33179645 A G 22 GENIC homozygous 969572753 5 33180034 33180035 C T 10 GENIC homozygous 969572754 5 33180442 33180443 C T 16 GENIC homozygous 969572755 5 33180660 33180661 T C 20 GENIC homozygous 969572756