chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 50379901 50379902 G A 26 GENIC homozygous 114797139 6 50380393 50380394 A T 11 GENIC homozygous 118553389 6 50380399 50380400 G T 11 GENIC homozygous 114797140 6 50380679 50380680 T C 25 GENIC homozygous 114797141 6 50381206 50381207 A G 35 GENIC homozygous 114797142 6 50381517 50381518 T A 42 GENIC homozygous 114797143 6 50381591 50381592 A G 27 GENIC homozygous 114797144 6 50381624 50381625 T A 25 GENIC homozygous 114797145 6 50382736 50382737 C G 35 GENIC homozygous 114797146 6 50383265 50383266 C A 37 GENIC homozygous 114797147 6 50383712 50383713 G A 23 GENIC homozygous 114797148 6 50383763 50383764 G T 26 GENIC homozygous 114797149 6 50384111 50384112 T C 36 GENIC homozygous 114797150 6 50384414 50384415 C A 23 GENIC homozygous 114797151 6 50384940 50384941 T C 44 GENIC homozygous 114797152 6 50385042 50385043 C T 21 GENIC homozygous 114797153 6 50385071 50385072 A G 21 GENIC homozygous 114797154 6 50385527 50385528 T C 34 GENIC homozygous 114797155 6 50385647 50385648 G A 24 GENIC homozygous 114797156 6 50386112 50386113 A G 21 GENIC homozygous 114797157 6 50386841 50386842 A G 19 GENIC homozygous 114797158 6 50386910 50386911 G A 9 GENIC homozygous 114797159 6 50387011 50387012 T C 6 GENIC homozygous 114797160 6 50387110 50387111 C T 13 GENIC homozygous 114797161 6 50387236 50387237 C T 15 GENIC homozygous 114797162 6 50387692 50387693 A G 33 GENIC homozygous 114797163