chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 55901987 55901988 C T 20 GENIC possibly homozygous 116935061 10 55902848 55902849 T C 31 GENIC homozygous 116782972 10 55903222 55903223 C T 21 GENIC homozygous 116782976 10 55903350 55903351 C G 32 GENIC homozygous 116782978 10 55903608 55903609 G A 21 GENIC homozygous 116935063 10 55903861 55903862 C T 28 GENIC homozygous 116782982 10 55904102 55904103 A T 15 GENIC homozygous 116782984 10 55904566 55904567 C T 21 GENIC possibly homozygous 116935065 10 55904840 55904841 G A 16 GENIC homozygous 116935067 10 55905489 55905490 A G 17 GENIC homozygous 116935069 10 55905639 55905640 C T 21 GENIC homozygous 116935071 10 55906082 55906083 T G 36 GENIC homozygous 116782988 10 55906999 55907000 G A 17 GENIC homozygous 116935073 10 55909581 55909582 G T 15 GENIC homozygous 116935075 10 55909897 55909898 T C 30 GENIC homozygous 116783002 10 55915554 55915555 T C 13 GENIC homozygous 116783004 10 55917048 55917049 T C 27 GENIC homozygous 116935077 10 55923158 55923159 A G 31 GENIC homozygous 116783012 10 55924238 55924239 G A 25 GENIC homozygous 116783014 10 55924684 55924685 C A 11 GENIC homozygous 116783016 10 55926591 55926592 A C 32 GENIC homozygous 116783018 10 55913897 55913898 C T 10 GENIC homozygous 117179234