chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 56556100 56556101 T G 44 GENIC possibly homozygous 807421955 5 56557394 56557395 T C 57 GENIC homozygous 807421956 5 56558838 56558839 A T 61 GENIC homozygous 807421957 5 56559036 56559037 A G 54 GENIC homozygous 807421958 5 56559866 56559867 T C 43 GENIC homozygous 807421959 5 56560069 56560070 G A 14 GENIC possibly homozygous 807421960 5 56560163 56560164 C T 38 GENIC heterozygous 807421961 5 56560756 56560757 C T 81 GENIC heterozygous 807421962 5 56560783 56560784 A G 34 GENIC possibly homozygous 807421963 5 56560795 56560796 C T 45 GENIC heterozygous 807421964 5 56560802 56560803 C T 53 GENIC heterozygous 807421965 5 56560813 56560814 A G 39 GENIC heterozygous 807421966 5 56560931 56560932 C T 39 GENIC homozygous 807421967 5 56561004 56561005 A G 49 GENIC homozygous 807421968 5 56561140 56561141 G T 32 GENIC homozygous 807421969 5 56561901 56561902 A T 33 GENIC heterozygous 807421970 5 56561911 56561912 T A 41 GENIC heterozygous 807421971 5 56561931 56561932 T A 37 GENIC heterozygous 807421972 5 56562080 56562081 C T 35 GENIC possibly homozygous 807421973 5 56562096 56562097 G A 43 GENIC possibly homozygous 807421974 5 56562546 56562547 T C 60 GENIC homozygous 807421975 5 56563187 56563188 T C 46 GENIC homozygous 807421976 5 56563307 56563308 T A 48 GENIC homozygous 807421977 5 56563622 56563623 A T 36 GENIC possibly homozygous 807421978 5 56563782 56563783 A C 43 GENIC homozygous 807421979 5 56564353 56564354 C A 53 GENIC homozygous 807421980 5 56564512 56564513 C T 60 GENIC homozygous 807421981 5 56565143 56565144 T G 21 GENIC homozygous 807421982 5 56565211 56565212 A G 17 GENIC homozygous 807421983 5 56565391 56565392 C T 36 GENIC possibly homozygous 807421984 5 56565837 56565838 C T 71 GENIC homozygous 807421985 5 56566169 56566170 T C 36 GENIC homozygous 807421986 5 56566213 56566214 G A 28 GENIC possibly homozygous 807421987