chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 103341720 103341721 C T 34 GENIC homozygous 116959800 10 103342156 103342157 T G 24 GENIC homozygous 116832568 10 103342420 103342421 T C 25 GENIC homozygous 116832570 10 103344088 103344089 G A 42 GENIC homozygous 116959802 10 103344609 103344610 T C 19 GENIC homozygous 116832578 10 103345519 103345520 T C 23 GENIC homozygous 116832586 10 103345560 103345561 A C 24 GENIC homozygous 116832588 10 103346174 103346175 C A 15 GENIC homozygous 116959804 10 103346599 103346600 A G 29 GENIC homozygous 116832592 10 103346917 103346918 C T 22 GENIC homozygous 116832596 10 103347004 103347005 G A 28 GENIC homozygous 116832598 10 103347028 103347029 G A 31 GENIC homozygous 116959806 10 103347115 103347116 C T 33 GENIC homozygous 116832600 10 103347641 103347642 C T 41 GENIC homozygous 116959808 10 103347915 103347916 T C 36 GENIC homozygous 116832604 10 103348033 103348034 C T 35 GENIC homozygous 116959810 10 103348636 103348637 A G 28 GENIC homozygous 116959812 10 103348731 103348732 C T 25 GENIC homozygous 116959814 10 103348744 103348745 T C 25 GENIC homozygous 116832612 10 103348839 103348840 T C 25 GENIC homozygous 116832614 10 103349073 103349074 C G 25 GENIC homozygous 116959816 10 103349115 103349116 T A 37 GENIC homozygous 116959818 10 103349199 103349200 C T 36 GENIC homozygous 116832618 10 103349344 103349345 A G 32 GENIC homozygous 116832620 10 103349689 103349690 T C 25 GENIC homozygous 116832622 10 103349901 103349902 A G 34 GENIC homozygous 116959820 10 103350317 103350318 G T 34 GENIC homozygous 116959822 10 103350447 103350448 G A 25 GENIC homozygous 116832632