chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 118373922 118373923 T C 39 GENIC homozygous 112822032 4 118374133 118374134 G C 31 GENIC homozygous 112822034 4 118376098 118376099 C G 32 GENIC homozygous 112822036 4 118376393 118376394 T C 45 GENIC homozygous 112822038 4 118379159 118379160 C T 44 GENIC homozygous 112822042 4 118379280 118379281 A G 59 GENIC homozygous 112822044 4 118379654 118379655 C T 41 GENIC homozygous 112822046 4 118381281 118381282 C T 48 GENIC homozygous 112822048 4 118381863 118381864 G T 37 GENIC homozygous 112822050 4 118382018 118382019 C T 47 GENIC homozygous 112822052 4 118382548 118382549 C A 22 GENIC possibly homozygous 112822056 4 118382559 118382560 C A 29 GENIC homozygous 112822058 4 118382709 118382710 G A 52 GENIC homozygous 112822060 4 118382726 118382727 C T 53 GENIC homozygous 112822062 4 118382899 118382900 C T 51 GENIC homozygous 112822064 4 118384185 118384186 G T 40 GENIC homozygous 112822066 4 118384405 118384406 T A 15 GENIC homozygous 112822068 4 118384452 118384453 C G 18 GENIC homozygous 112822070