chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 109396476 109396477 A G 17 GENIC homozygous 51599162 10 109398234 109398235 G A 15 GENIC possibly homozygous 51956481 10 109398388 109398389 T C 9 GENIC heterozygous 51599163 10 109399760 109399761 T C 25 GENIC homozygous 51599165 10 109399877 109399878 G A 20 GENIC possibly homozygous 51599166 10 109400303 109400304 C G 10 GENIC possibly homozygous 51956484 10 109401070 109401071 A G 8 GENIC homozygous 51599167 10 109401200 109401201 A T 9 GENIC homozygous 51599168 10 109401421 109401422 T C 28 GENIC possibly homozygous 51599169 10 109402180 109402181 C T 19 GENIC homozygous 51599170 10 109402201 109402202 T C 19 GENIC possibly homozygous 51599171 10 109402277 109402278 A AT 25 GENIC possibly homozygous 51599172 10 109402340 109402341 G GTGTGTGCA 3 GENIC homozygous 51956487 10 109402611 109402612 C A 27 GENIC possibly homozygous 51599173 10 109403437 109403438 A G 17 GENIC possibly homozygous 51599174 10 109403734 109403735 T C 4 GENIC homozygous 51599175