chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 33176139 33176140 C T 39 GENIC homozygous 929008654 5 33177051 33177052 A C 19 GENIC homozygous 929008655 5 33177272 33177273 C T 40 GENIC heterozygous 929008656 5 33177642 33177643 G A 48 GENIC heterozygous 929008657 5 33177751 33177752 G T 44 GENIC heterozygous 929008658 5 33177776 33177777 T C 61 GENIC heterozygous 929008659 5 33177853 33177854 A G 51 GENIC heterozygous 929008660 5 33177994 33177995 G A 38 GENIC heterozygous 929008661 5 33178007 33178008 G A 39 GENIC heterozygous 929008662 5 33178076 33178077 C A 66 GENIC heterozygous 929008663 5 33178080 33178081 G A 64 GENIC heterozygous 929008664 5 33178083 33178084 G A 65 GENIC heterozygous 929008665 5 33178112 33178113 G A 59 GENIC heterozygous 929008666 5 33178159 33178160 C T 50 GENIC heterozygous 929008667 5 33179644 33179645 A G 25 GENIC homozygous 929008668 5 33180034 33180035 C T 17 GENIC homozygous 929008669 5 33180442 33180443 C T 14 GENIC homozygous 929008670 5 33180660 33180661 T C 21 GENIC homozygous 929008671