chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 33176139 33176140 C T 16 GENIC homozygous 934997014 5 33177051 33177052 A C 22 GENIC homozygous 934997015 5 33177642 33177643 G A 23 GENIC heterozygous 934997016 5 33177668 33177669 C A 26 GENIC heterozygous 934997017 5 33177751 33177752 G T 21 GENIC heterozygous 934997018 5 33177776 33177777 T C 25 GENIC heterozygous 934997019 5 33177853 33177854 A G 23 GENIC heterozygous 934997020 5 33178159 33178160 C T 22 GENIC heterozygous 934997021 5 33178210 33178211 C G 20 GENIC heterozygous 934997022 5 33178216 33178217 G A 16 GENIC heterozygous 934997023 5 33178221 33178222 A G 16 GENIC heterozygous 934997024 5 33178226 33178227 A G 16 GENIC heterozygous 934997025 5 33178231 33178232 G T 14 GENIC heterozygous 934997026 5 33179644 33179645 A G 9 GENIC homozygous 934997027 5 33180442 33180443 C T 12 GENIC homozygous 934997028 5 33180660 33180661 T C 4 GENIC homozygous 934997029