chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	235311777	235311778	C	T	39	GENIC	homozygous	110314727
2	235311784	235311785	C	G	38	GENIC	homozygous	110314729
2	235312193	235312194	C	A	58	GENIC	homozygous	110314733
2	235312273	235312274	A	T	38	GENIC	possibly homozygous	110314735
2	235312393	235312394	T	A	79	GENIC	homozygous	110314737
2	235312602	235312603	G	A	44	GENIC	homozygous	110314739
2	235312610	235312611	C	G	44	GENIC	homozygous	110314741
2	235312702	235312703	G	A	46	GENIC	homozygous	110314743
2	235315650	235315651	A	T	22	GENIC	homozygous	120220123
2	235320628	235320629	G	T	26	GENIC	homozygous	110314745
2	235324347	235324348	G	C	56	GENIC	homozygous	110314747
2	235325076	235325077	T	C	63	GENIC	homozygous	110314749
2	235326623	235326624	G	A	43	GENIC	homozygous	110314751
2	235326642	235326643	G	A	41	GENIC	homozygous	110314753
2	235326678	235326679	T	C	50	GENIC	homozygous	110314755
2	235326679	235326680	G	A	51	GENIC	homozygous	110314757
2	235326915	235326916	A	G	85	GENIC	homozygous	110314763
2	235326948	235326949	A	G	71	GENIC	homozygous	110314765
2	235326955	235326956	G	A	67	GENIC	homozygous	110314767
2	235327001	235327002	A	C	40	GENIC	homozygous	110314769
2	235327135	235327136	G	A	42	GENIC	homozygous	110314771