chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 129555447 129555448 A T 19 GENIC homozygous 143959165 5 129555924 129555924 T 11 GENIC homozygous 143943630 5 129557428 129557429 C T 19 GENIC homozygous 143959166 5 129560532 129560533 A G 22 GENIC homozygous 143959167 5 129561531 129561532 G A 23 GENIC homozygous 143959168 5 129563767 129563768 T G 17 GENIC homozygous 143959169 5 129564762 129564763 A T 22 GENIC homozygous 143959170 5 129566807 129566808 T C 29 GENIC homozygous 143959171 5 129566960 129566961 T C 23 GENIC homozygous 143959172 5 129568755 129568756 T C 20 GENIC possibly homozygous 143959173 5 129569613 129569614 A C 16 GENIC possibly homozygous 141761877 5 129570504 129570505 C A 19 GENIC homozygous 143959174 5 129570974 129570975 C T 17 GENIC homozygous 143959175 5 129571138 129571138 CTA 17 GENIC possibly homozygous 143943631 5 129573245 129573246 T C 22 GENIC homozygous 143959176 5 129573292 129573293 T C 21 GENIC homozygous 143959177 5 129574528 129574529 C G 24 GENIC homozygous 143959178 5 129575186 129575187 G A 14 GENIC homozygous 143959179 5 129564859 129564860 C G 16 GENIC homozygous 137620203 5 129556596 129556597 A G 15 GENIC homozygous 137620201 5 129558535 129558536 T C 22 GENIC homozygous 137620202 5 129572370 129572371 T 7 GENIC homozygous 137341081