chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 157791822 157791823 T C 27 GENIC homozygous 793723468 4 157791833 157791834 T C 23 GENIC homozygous 793723469 4 157791845 157791846 T A 22 GENIC possibly homozygous 793723470 4 157791851 157791852 T C 25 GENIC heterozygous 793723471 4 157791863 157791864 A T 25 GENIC heterozygous 793723472 4 157792271 157792272 G A 30 GENIC homozygous 793723473 4 157793017 157793018 G T 28 GENIC possibly homozygous 793723474 4 157795166 157795167 C T 27 GENIC homozygous 793723475 4 157796662 157796663 T C 20 GENIC homozygous 793723476 4 157796750 157796751 C T 25 GENIC homozygous 793723477 4 157797124 157797125 G A 39 GENIC homozygous 793723478 4 157797798 157797799 G T 23 GENIC heterozygous 793723479 4 157797801 157797802 C T 23 GENIC heterozygous 793723480 4 157797854 157797855 T G 25 GENIC possibly homozygous 793723481 4 157798356 157798357 T G 29 GENIC homozygous 793723482