chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 154514251 154514255 CGGC ---- 17 GENIC homozygous 692163214 3 154514259 154514260 C T 20 GENIC homozygous 526947672 3 154514276 154514277 T G 22 GENIC homozygous 524596844 3 154514414 154514415 A AGTCT 23 GENIC homozygous 692163215 3 154515300 154515301 G A 19 GENIC homozygous 524596845 3 154515475 154515476 G A 20 GENIC homozygous 524596846 3 154515627 154515628 G A 36 GENIC homozygous 524596847 3 154515681 154515682 T A 26 GENIC homozygous 524596848 3 154515884 154515885 A G 14 GENIC homozygous 524596849 3 154516260 154516261 T C 42 GENIC homozygous 524596850 3 154516490 154516491 A T 25 GENIC homozygous 524596851 3 154516884 154516885 A G 49 GENIC homozygous 524596852 3 154516887 154516888 G A 49 GENIC possibly homozygous 524596853 3 154517156 154517157 A G 28 GENIC homozygous 524596854 3 154517166 154517167 T G 28 GENIC homozygous 524596855 3 154517351 154517352 G - 41 GENIC homozygous 692163216 3 154517632 154517633 G - 25 GENIC homozygous 692163217 3 154517898 154517899 T C 20 GENIC homozygous 524596856 3 154518068 154518069 G A 37 GENIC homozygous 524596857 3 154518158 154518159 T TA 40 GENIC homozygous 692163218 3 154519184 154519185 C CA 8 GENIC heterozygous 692163219 3 154519184 154519185 C CCA 8 GENIC heterozygous 692163220 3 154519630 154519636 TCCCTC ------ 17 GENIC homozygous 692163221 3 154519645 154519646 C G 24 GENIC heterozygous 524596858 3 154519651 154519652 G C 22 GENIC heterozygous 524596859 3 154519872 154519873 A C 28 GENIC homozygous 524596860 3 154519897 154519899 TT -- 23 GENIC homozygous 692163222 3 154519985 154519986 A G 37 GENIC homozygous 524596861 3 154520058 154520059 T C 32 GENIC homozygous 524596862 3 154520079 154520080 G C 34 GENIC homozygous 524596863 3 154521686 154521687 C T 31 GENIC homozygous 524596864 3 154521930 154521931 A AC 20 GENIC heterozygous 692163224 3 154522134 154522135 A G 25 GENIC homozygous 524596865