chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 71011809 71011810 T G 4 GENIC homozygous 108449769 X 71011810 71011811 C T 4 GENIC homozygous 108449771 X 71011812 71011813 A C 4 GENIC homozygous 108449773 X 71021227 71021228 G A 3 GENIC homozygous 108273182 X 71045054 71045055 C A 16 GENIC homozygous 108273192 X 71045055 71045056 A C 16 GENIC homozygous 108273194 X 71045146 71045147 C G 13 GENIC homozygous 108273196 X 71045173 71045174 C G 9 GENIC homozygous 108273198 X 71045304 71045305 G T 8 GENIC homozygous 108273200 X 71045530 71045531 C T 5 GENIC homozygous 108273202 X 71045535 71045536 G A 5 GENIC homozygous 108273204 X 71045568 71045569 T A 13 GENIC homozygous 108273208 X 71045934 71045935 G C 3 GENIC homozygous 108449783 X 71051443 71051444 A C 12 GENIC homozygous 108273210 X 71051476 71051477 G A 7 GENIC homozygous 108391215 X 71051494 71051495 G A 6 GENIC homozygous 108391217 X 71051497 71051498 C A 7 GENIC homozygous 108391219 X 71051506 71051507 G A 6 GENIC homozygous 108391221 X 71051546 71051547 G A 6 GENIC homozygous 108449787 X 71051547 71051548 A G 6 GENIC homozygous 108391225 X 71051557 71051558 C T 7 GENIC homozygous 108273212 X 71079576 71079577 C T 3 GENIC homozygous 108501755 X 71079583 71079584 G T 3 GENIC homozygous 108501757 X 71072405 71072406 A C 8 GENIC homozygous 108677228 X 71079531 71079532 G T 5 GENIC homozygous 108677229 X 71079569 71079570 C A 3 GENIC homozygous 108596362