chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	235311928	235311929	A	C	16	GENIC	homozygous	110314731
2	235312193	235312194	C	A	7	GENIC	homozygous	110314733
2	235312393	235312394	T	A	11	GENIC	homozygous	110314737
2	235312602	235312603	G	A	11	GENIC	homozygous	110314739
2	235312610	235312611	C	G	7	GENIC	homozygous	110314741
2	235312702	235312703	G	A	16	GENIC	homozygous	110314743
2	235320628	235320629	G	T	17	GENIC	homozygous	110314745
2	235322702	235322703	G	T	5	GENIC	homozygous	125608868
2	235322726	235322727	G	A	11	GENIC	homozygous	125608869
2	235322769	235322770	G	T	15	GENIC	homozygous	125608870
2	235322774	235322775	G	A	17	GENIC	homozygous	125608871
2	235324347	235324348	G	C	29	GENIC	homozygous	110314747
2	235325076	235325077	T	C	27	GENIC	homozygous	110314749
2	235326623	235326624	G	A	14	GENIC	homozygous	110314751
2	235326642	235326643	G	A	11	GENIC	homozygous	110314753
2	235326840	235326841	C	T	16	GENIC	homozygous	110314759
2	235327001	235327002	A	C	14	GENIC	homozygous	110314769
2	235327135	235327136	G	A	24	GENIC	homozygous	110314771