chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 60929070 60929071 A T 23 GENIC homozygous 574772192 2 60929086 60929087 T C 23 GENIC homozygous 574772193 2 60929211 60929212 T TTA 9 GENIC homozygous 713666183 2 60929265 60929266 T G 15 GENIC homozygous 574772194 2 60929886 60929887 T C 38 GENIC homozygous 573644715 2 60930547 60930548 A G 19 GENIC homozygous 573644716 2 60930719 60930720 G A 19 GENIC homozygous 573644717 2 60930858 60930859 A G 22 GENIC homozygous 573644718 2 60931211 60931212 A T 13 GENIC homozygous 573644719 2 60931743 60931744 T A 29 GENIC homozygous 573644720 2 60931898 60931899 T C 29 GENIC homozygous 573644721 2 60932121 60932122 T A 37 GENIC homozygous 573644722 2 60932183 60932184 A G 23 GENIC homozygous 573644723 2 60932689 60932690 C T 17 GENIC homozygous 573644724 2 60932703 60932704 A G 15 GENIC homozygous 573644725 2 60933003 60933004 A AACACACACAC 23 GENIC homozygous 713666184 2 60933032 60933033 G A 31 GENIC homozygous 573644726 2 60933039 60933040 A AACACAC 29 GENIC homozygous 713666186 2 60933111 60933112 A C 17 GENIC homozygous 573644727 2 60933259 60933260 C T 26 GENIC homozygous 573644728