chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 4054804 4054805 T TTTTTG 45 GENIC homozygous 45374702 20 4054805 4054806 T TTTTG 45 GENIC homozygous 45374703 20 4054808 4054809 T TG 43 GENIC possibly homozygous 45374704 20 4055152 4055153 C CAA 43 GENIC homozygous 45374705 20 4055723 4055724 C T 41 GENIC homozygous 45374706 20 4056308 4056309 T C 33 GENIC homozygous 45374707 20 4056881 4056882 A G 32 GENIC homozygous 45374708 20 4058346 4058347 G A 31 GENIC homozygous 45374710 20 4058585 4058586 C T 35 GENIC homozygous 45374711 20 4059105 4059106 C T 43 GENIC homozygous 45374712 20 4059249 4059250 G A 46 GENIC homozygous 45374713 20 4059351 4059352 A ATGTGTGTGTGTG 10 GENIC homozygous 45374714 20 4059429 4059430 A G 21 GENIC homozygous 45374715 20 4059816 4059817 C T 35 GENIC possibly homozygous 45374716 20 4060055 4060056 C T 29 GENIC homozygous 45374717 20 4060099 4060100 A - 27 GENIC homozygous 45374718 20 4060140 4060141 G C 42 GENIC homozygous 45374719 20 4060177 4060178 C T 34 GENIC homozygous 45374720 20 4060227 4060228 T A 29 GENIC homozygous 45374721 20 4060353 4060354 C T 36 GENIC homozygous 45374722 20 4060853 4060854 C T 27 GENIC homozygous 45374723