chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 60929070 60929071 A T 20 GENIC homozygous 626962757 2 60929086 60929087 T C 20 GENIC homozygous 626962758 2 60929211 60929212 T TTA 20 GENIC homozygous 743655061 2 60929265 60929266 T G 23 GENIC homozygous 626962759 2 60929886 60929887 T C 30 GENIC homozygous 626962760 2 60930547 60930548 A G 38 GENIC homozygous 626962761 2 60930719 60930720 G A 26 GENIC homozygous 626962762 2 60930858 60930859 A G 18 GENIC homozygous 626962763 2 60931211 60931212 A T 29 GENIC homozygous 626962764 2 60931743 60931744 T A 24 GENIC homozygous 626962765 2 60931898 60931899 T C 18 GENIC homozygous 626962766 2 60932121 60932122 T A 30 GENIC homozygous 626962767 2 60932183 60932184 A G 21 GENIC homozygous 626962768 2 60932689 60932690 C T 25 GENIC homozygous 626962769 2 60932703 60932704 A G 25 GENIC homozygous 626962770 2 60933003 60933004 A AACACACACAC 10 GENIC homozygous 743655062 2 60933032 60933033 G A 13 GENIC homozygous 626962771 2 60933039 60933040 A AACACAC 12 GENIC homozygous 743655064 2 60933111 60933112 A C 20 GENIC homozygous 626962772 2 60933259 60933260 C T 19 GENIC homozygous 626962773