chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 47653380 47653381 T C 29 GENIC homozygous 653923928 11 47653515 47653516 A G 27 GENIC homozygous 653923929 11 47653542 47653543 C T 36 GENIC homozygous 653923930 11 47653543 47653544 A G 37 GENIC homozygous 653923931 11 47653625 47653626 A G 44 GENIC homozygous 653923932 11 47653743 47653744 C T 43 GENIC homozygous 653923933 11 47654069 47654070 C T 23 GENIC homozygous 653923934 11 47654989 47654990 C T 24 GENIC homozygous 653923935 11 47655157 47655158 T G 25 GENIC homozygous 653923936 11 47655346 47655347 T G 32 GENIC homozygous 653923937 11 47655466 47655467 G - 23 GENIC possibly homozygous 759414864 11 47655508 47655509 T TA 19 GENIC homozygous 759414865 11 47655542 47655543 T C 24 GENIC homozygous 653923938 11 47655911 47655912 T C 13 GENIC homozygous 653923939 11 47655928 47655929 C T 13 GENIC homozygous 653923940 11 47655929 47655930 A G 13 GENIC homozygous 653923941 11 47656018 47656019 T C 10 GENIC homozygous 653923942 11 47656140 47656141 C G 13 GENIC homozygous 653923943 11 47656143 47656144 T - 14 GENIC homozygous 759414866 11 47656155 47656156 T C 17 GENIC homozygous 653923944 11 47656192 47656193 G A 21 GENIC homozygous 653923945 11 47656245 47656246 T C 16 GENIC homozygous 653923946