chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 17284816 17284817 C T 20 GENIC homozygous 976955036 14 17285052 17285053 T A 20 GENIC homozygous 976955037 14 17285058 17285059 C T 20 GENIC homozygous 976955038 14 17285203 17285204 G C 17 GENIC homozygous 976955039 14 17285876 17285877 C G 10 GENIC homozygous 976955040 14 17285881 17285882 C T 13 GENIC homozygous 976955041 14 17286040 17286041 G A 14 GENIC homozygous 976955042 14 17286108 17286109 A C 11 GENIC homozygous 976955043 14 17286695 17286696 C T 14 GENIC possibly homozygous 976955044 14 17286768 17286769 T A 13 GENIC homozygous 976955045 14 17286858 17286859 T C 7 GENIC homozygous 976955046 14 17287036 17287037 C A 4 GENIC homozygous 976955047 14 17287048 17287049 C T 3 GENIC homozygous 976955048 14 17287819 17287820 T G 24 GENIC homozygous 976955049 14 17287924 17287925 C T 16 GENIC homozygous 976955050 14 17288175 17288176 G A 33 GENIC homozygous 976955051 14 17289618 17289619 G A 28 GENIC homozygous 976955052 14 17289632 17289633 A G 27 GENIC homozygous 976955053 14 17289774 17289775 G A 15 GENIC homozygous 976955054 14 17289787 17289788 A G 14 GENIC homozygous 976955055 14 17290250 17290251 T C 7 GENIC homozygous 976955056 14 17291087 17291088 C T 10 GENIC homozygous 976955057 14 17291227 17291228 C A 17 GENIC homozygous 976955058 14 17291252 17291253 T C 20 GENIC homozygous 976955059 14 17291482 17291483 G C 20 GENIC homozygous 976955060 14 17292019 17292020 C T 17 GENIC homozygous 976955061 14 17292286 17292287 G C 26 GENIC homozygous 976955062 14 17292316 17292317 C T 30 GENIC homozygous 976955063 14 17292947 17292948 G T 16 GENIC homozygous 976955064 14 17292950 17292951 C T 16 GENIC homozygous 976955065 14 17293291 17293292 T C 22 GENIC homozygous 976955066 14 17293391 17293392 A G 15 GENIC homozygous 976955067 14 17293488 17293489 A G 11 GENIC homozygous 976955068 14 17295024 17295025 T C 30 GENIC homozygous 976955069 14 17296966 17296967 G A 23 GENIC homozygous 976955070