chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 150685716 150685717 T C 26 GENIC homozygous 941112630 5 150687272 150687273 C T 23 GENIC homozygous 941112631 5 150690664 150690665 G A 31 GENIC homozygous 941112632 5 150690906 150690907 T C 38 GENIC homozygous 941112633 5 150691388 150691389 C T 9 GENIC homozygous 941112634 5 150691794 150691795 T C 30 GENIC homozygous 941112635 5 150692118 150692119 T A 4 GENIC homozygous 941112636 5 150692120 150692121 G C 4 GENIC homozygous 941112637 5 150692122 150692123 T C 8 GENIC homozygous 941112638 5 150692332 150692333 G A 32 GENIC homozygous 941112639 5 150692912 150692913 C T 20 GENIC homozygous 941112640 5 150694695 150694696 C T 19 GENIC homozygous 941112641 5 150695760 150695761 C T 24 GENIC homozygous 941112642 5 150696424 150696425 T C 16 GENIC homozygous 941112643 5 150696850 150696851 G A 11 GENIC homozygous 941112644 5 150698973 150698974 C T 28 GENIC homozygous 941112645 5 150699625 150699626 G A 9 GENIC homozygous 941112646 5 150701338 150701339 C T 37 GENIC homozygous 941112647 5 150701466 150701467 T C 26 GENIC homozygous 941112648 5 150703071 150703072 A C 25 GENIC homozygous 941112649