chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 159705062 159705063 G C 55 GENIC homozygous 783387924 X 159705254 159705255 G A 94 GENIC possibly homozygous 783387925 X 159705374 159705375 C T 81 GENIC homozygous 783387926 X 159707465 159707466 A G 38 GENIC homozygous 783387927 X 159708024 159708025 A G 53 GENIC homozygous 783387928 X 159709077 159709078 G A 52 GENIC homozygous 783387929 X 159710314 159710315 G A 77 GENIC homozygous 783387930 X 159711196 159711197 A G 28 GENIC heterozygous 783387931 X 159711476 159711477 G A 67 GENIC homozygous 783387932 X 159712372 159712373 T C 67 GENIC homozygous 783387933 X 159712457 159712458 A G 80 GENIC homozygous 783387934