chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 159703910 159703911 T C 7 GENIC homozygous 995761585 X 159704918 159704919 C G 16 GENIC homozygous 995761586 X 159704970 159704971 C G 15 GENIC homozygous 995761587 X 159705254 159705255 G A 14 GENIC possibly homozygous 995761588 X 159705374 159705375 C T 8 GENIC possibly homozygous 995761589 X 159705880 159705881 T C 9 GENIC homozygous 995761590 X 159707465 159707466 A G 15 GENIC possibly homozygous 995761591 X 159708024 159708025 A G 16 GENIC homozygous 995761592 X 159709077 159709078 G A 16 GENIC homozygous 995761593 X 159710314 159710315 G A 16 GENIC possibly homozygous 995761594 X 159711476 159711477 G A 7 GENIC homozygous 995761595 X 159712372 159712373 T C 8 GENIC homozygous 995761596 X 159712457 159712458 A G 9 GENIC homozygous 995761597