chr start stop reference nuc variant nuc depth genic status zygosity variant ID 20 4054805 4054806 T TTTTG 10 GENIC homozygous 45374703 20 4055152 4055153 C CAA 23 GENIC homozygous 45374705 20 4055723 4055724 C T 8 GENIC homozygous 45374706 20 4056308 4056309 T C 12 GENIC homozygous 45374707 20 4056881 4056882 A G 18 GENIC homozygous 45374708 20 4058346 4058347 G A 21 GENIC homozygous 45374710 20 4058585 4058586 C T 21 GENIC homozygous 45374711 20 4059105 4059106 C T 21 GENIC homozygous 45374712 20 4059249 4059250 G A 31 GENIC homozygous 45374713 20 4059351 4059352 A ATGTGTGTGTGTG 7 GENIC homozygous 45374714 20 4059429 4059430 A G 18 GENIC homozygous 45374715 20 4059816 4059817 C T 13 GENIC homozygous 45374716 20 4060055 4060056 C T 19 GENIC homozygous 45374717 20 4060099 4060100 A - 18 GENIC homozygous 45374718 20 4060140 4060141 G C 17 GENIC homozygous 45374719 20 4060177 4060178 C T 15 GENIC homozygous 45374720 20 4060227 4060228 T A 12 GENIC homozygous 45374721 20 4060353 4060354 C T 16 GENIC homozygous 45374722 20 4060853 4060854 C T 14 GENIC homozygous 45374723